Lediga jobb Antaros Medical AB i Göteborg

Would you like to work as a manager in a growing company devoted to making a real difference in drug development through ground-breaking imaging? How about working in a leadership role where you can impact the organisation and the growth journey we are on? In a company that is constantly moving forward, with great science, people and a great atmosphere? If this catches your interest, you should continue reading.
At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development. We are currently around 140 employees working at our offices in Sweden in Mölndal, Uppsala, Lund and in the US and UK, and we are continuously growing. As a part of our growth journey, we are looking for a Head of Clinical Operations who will lead the department.
This position is a senior management role in the operational organisation where you will be responsible for the Clinical Operations Department consisting of a team of Project Managers and Project Coordinators including the Line Managers for these groups. As Head of Clinical Operations, you will be responsible for the department and its processes, ensuring that projects run smoothly through efficient workflows, and for implementing Antaros Medical's strategy within the department. You will also be part of the Operational Management Team. You will be reporting to the COO, and the role will be based in Uppsala or Mölndal.
As Head of Clinical Operations your main responsibilities will be:
Provide strategic leadership and guidance to the Clinical Operations Department, fostering a high-performing culture through support in mentoring, coaching, development, and recruitment initiatives in collaboration with the Line Managers
Ensure that projects are managed in a smooth, streamlined and efficient way by continuously improving workflows, removing complexity and supporting best practices across teams
Leading the day-to-day operations ensuring operational challenges and changes are addressed
Improve operational efficiency and develop short-term and long-term strategies for the Clinical Operations Department that aligns with company strategy and goals
Keep oversight of all our clinical trials in collaboration with the Project Managers, ensuring they are delivered to timelines, agreed budget, and high quality and in accordance with internal and client’s SOPs and ICH/GCP
Collaborate with our Compliance organisation, to ensure efficient and compliant workflows
Actively collaborate with fellow managers in the Operational Management Team to ensure streamlined and efficient cooperation between departments within Operations
Represent Clinical Operations in customer meetings, and audits and inspections
Assist the COO in building the operational platform and in daily activities as applicable

Who you are
We believe that you are a committed, strategic, and forward-thinking leader who thrives in a dynamic and rapidly evolving environment. You are passionate about building and leading teams, and you get energy from developing people, collaborating with colleagues and growing an organization. You have a strong drive to identify smarter, more efficient ways of working, and you enjoy translating vision into scalable structures and processes. You combine excellent collaboration skills with a team-oriented mindset to engage colleagues and clients alike. You are used to handling multiple priorities while delivering high-quality results - and you believe that continuous improvement is a natural part of success. And last but not least, you value having fun while doing meaningful work.
Requirements:
University degree in life sciences
At least 5 years experience in project management in clinical trials, preferably in a CRO setting or as a consultant
3-5 years experience from a management role, preferably from a CRO setting
Strong understanding of ICH-GCP and other relevant regulations and guidelines in relation to clinical trials
Demonstrated experience in leading quality improvement initiatives
Experience from internal and external audits is beneficial
Strong understanding of the full drug development process
Excellent written and verbal communication skills in English

More information
For more information about the position, please contact Kerstin Heurling at [email protected]
Please submit your application via this link with your CV included, no later than August 15, 2025. Interviews might be performed throughout the application period. We only accept applications via our recruitment system, Teamtailor. The recruitment is handled by Antaros Medical.
About Antaros Medical

At Antaros Medical, we combine ground-breaking imaging with profound experience in drug development and deep knowledge of disease mechanisms. We specialize in cardiorenal and metabolic disease. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as the Innovative Medicines Initiative (IMI).
Antaros Medical delivers both small, complex, mechanistic studies as well as large, streamlined multi-center clinical trials utilizing our innovative imaging methods. Our global headquarters are based in Sweden. If you want to find out more about our company, please visit: www.antarosmedical.com
Our culture is our people, and our values make us everything that we are. Please feel free to have a look at our Culture Handbook to get to know us even better:Our culture – Antaros Medical. Visa mindre

Does working with legal coordination, administration, and assistance in a dynamic environment intrigue you? Are you interested in joining an innovative company within the global Life Science sector where you can support legal processes mainly within contracts? If you're a driven law student who thrives on producing results through structure and collaboration, then keep reading.
At Antaros Medical, we prioritize competence, development, ideas, and solutions. Building strong relationships and trust is key to our success and having fun while doing meaningful work is equally important. With around 130 employees across our offices in Sweden (Mölndal, Uppsala, Lund) and the US, and continuous growth, we are now seeking a part-time Legal Assistant for administrative support in our legal department. The position is preferably based at our Mölndal office, but can be based in Uppsala for the right candidate.
Legal processes and documentation are vital for maintaining our competitive edge and adhering to industry regulations. As a part-time Legal Assistant, you'll support the Legal Director with administration, documentation, and general assistance in various legal processes. The position is part-time, corresponding to up to 8 hours per week depending on department’s needs and your availability.
Your main responsibilities will include:
Providing general administrative support and assistance within legal department to ensure efficient operations.
Managing, organizing, filing, and archiving various legal documents and contracts to support workflow and maintain operational effectiveness.
Supporting contractual processes
Other tasks as delegated

Who are we looking for? We believe that you are currently studying Law (Juristprogrammet) at a University in Sweden, with at least 2 semesters of performed studies in law school and at least 2 semesters left before graduation. You may have some experience working in a legal setting, focusing on service, administration, and/or compliance.
As a person, you excel in communication and enjoy interacting with others. You are known for your strong administrative skills, attention to detail, analytical thinking, and proactive mindset. The role requires a structured approach, flexibility, and an understanding of the broader implications of legal work. You are eager to learn new skills, develop your legal expertise, and contribute to the department's goals.
Requirements:
Current law studies at Juristprogrammet at a Swedish University
Fluent English language skills in speech and writing.

Are you interested?
Great! Please submit your application via the link below with your CV included, no later than May 18th, 2025. We will contact and interview candidates continuously throughout the recruitment process.
For more information about the position, please contact Sasha Dokmanovic, Legal Director, at [email protected] or Caroline Engvall, Chief Compliance Officer at [email protected].
We only accept applications through our recruitment system, Teamtailor, and the recruitment is managed directly by Antaros Medical.
About Antaros Medical
At Antaros Medical, we combine ground-breaking imaging with profound experience in drug development and deep knowledge of disease mechanisms. We are specialised in cardiorenal & metabolic diseases and oncology. We have a global network of collaboration partners and customers, including both Big Pharma and Biotech, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI) and COST.
Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden. If you want to find out more about our company, visit our website: www.antarosmedical.com.
Our culture is our people, and our values make us everything that we are. Please feel free to have a look upon our Culture Handbook to get to know us even better: Our culture – Antaros Medical. Visa mindre

Are you interested in HR coordination, administration, and assistance within a dynamic work environment? Would you like to work at an innovative company in the global Life Science sector, supporting recruitment and various HR processes? If you're a dedicated student who enjoys working in a structured manner and values teamwork, then you should continue reading.
At Antaros Medical, we prioritize competence, development, ideas, and solutions. Building strong relationships and maintaining trust are key to our success, just as much as having fun while doing a meaningful job. With approximately 130 employees across our offices in Mölndal, Uppsala, and Lund in Sweden, as well as in the US, our team is continuously expanding. As part of our growth journey, we are seeking a part-time HR Assistant to provide HR and recruitment administrative support.
We believe that robust HR processes are crucial for a thriving work environment, which includes recruiting and retaining our great staff. As a part-time HR Assistant, you will join our HR team, assisting with administration, documentation, and general support across various HR processes. You will also help coordinate recruitment and onboarding processes in collaboration with managers and other departments. The position is based at our Mölndal office, and you will be reporting to the VP, HR.
Your main responsibilities will include:
Providing general HR administrative support and assistance.
Managing various HR documentation.
Supporting our recruitment and onboarding processes.
Coordinating organizational engagement activities.

Who are we looking for? We are searching for someone currently studying HR or a related field at the university level, with at least one year left before graduation. You may have some initial experience in HR-related service, administration, and/or recruitment.
As an individual, you should excel in communication and interaction with others, enjoying producing results through support and collaboration. We also value strong administrative skills, an analytical and proactive mindset, and the ability to work in a broad HR setting, which requires a structured approach as well as flexibility and an understanding of the bigger picture.
Since we are committed to learning, development, and growth, we hope you will demonstrate a growth mindset, continually learning and building on both external and internal ideas, while keeping up with the latest news within the HR area. We want you to grow with us!
Requirements:
Current B.Sc. or M.Sc. studies in HR or equivalent.
Fluent English language skills in speech and writing.
At least 1 year of experience within recruitment

Are you interested? We would love to hear from you! Please submit your application through our recruitment system, Teamtailor, including your CV, no later than April 11, 2025. We will contact and interview candidates continuously throughout the recruitment process.
For more information about the position, please contact Sofia Löwstedt, VP HR, at [email protected].
This position is for part-time employment, corresponding to approx. 2 days per week, depending on our needs and your availability.

About Antaros Medical At Antaros Medical, we combine ground-breaking imaging with profound experience in drug development and deep knowledge of disease mechanisms. We are specialized in cardiorenal & metabolic disease. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI).
Antaros Medical delivers both small, complex, mechanistic studies as well as large, streamlined multi-center clinical trials utilizing our innovative imaging methods. Our global headquarters and analysis Corelab are based in Sweden. If you want to find out more about our company, please go to our website: www.antarosmedical.com.
Our culture is our people, and our values make us everything that we are. Please feel free to have a look upon our Culture Handbook to get to know us even better: Our culture – Antaros Medical. Visa mindre

Are you interested in HR coordination, administration, and assistance within a dynamic work environment? Would you like to work at an innovative company in the global Life Science sector, supporting recruitment and various HR processes? If you're a dedicated student who enjoys working in a structured manner and values teamwork, then you should continue reading.
At Antaros Medical, we prioritize competence, development, ideas, and solutions. Building strong relationships and maintaining trust are key to our success, just as much as having fun while doing a meaningful job. With approximately 130 employees across our offices in Mölndal, Uppsala, and Lund in Sweden, as well as in the US, our team is continuously expanding. As part of our growth journey, we are seeking a part-time HR Assistant to provide HR and recruitment administrative support.
We believe that robust HR processes are crucial for a thriving work environment, which includes recruiting and retaining our great staff. As a part-time HR Assistant, you will join our HR team, assisting with administration, documentation, and general support across various HR processes. You will also help coordinate recruitment and onboarding processes in collaboration with managers and other departments. The position is based at our Mölndal office, and you will be reporting to the VP, HR.
Your main responsibilities will include:
Providing general HR administrative support and assistance.
Managing various HR documentation.
Supporting our recruitment and onboarding processes.
Coordinating organizational engagement activities.

Who are we looking for? We are searching for someone currently studying HR or a related field at the university level, with at least one year left before graduation. You may have some initial experience in HR-related service, administration, and/or recruitment.
As an individual, you should excel in communication and interaction with others, enjoying producing results through support and collaboration. We also value strong administrative skills, an analytical and proactive mindset, and the ability to work in a broad HR setting, which requires a structured approach as well as flexibility and an understanding of the bigger picture.
Since we are committed to learning, development, and growth, we hope you will demonstrate a growth mindset, continually learning and building on both external and internal ideas, while keeping up with the latest news within the HR area. We want you to grow with us!
Requirements:
Current B.Sc. or M.Sc. studies in HR or equivalent.
Fluent English language skills in speech and writing.
Previous experience within recruitment (could be part-time)

Are you interested? We would love to hear from you! Please submit your application, in English, through our recruitment system, Teamtailor, including your CV, no later than April 3, 2025. We will contact and interview candidates continuously throughout the recruitment process.
For more information about the position, please contact Sofia Löwstedt, VP HR, at [email protected].
This position is for part-time employment, corresponding to approx. 2 days per week, depending on our needs and your availability.
About Antaros Medical At Antaros Medical, we combine ground-breaking imaging with profound experience in drug development and deep knowledge of disease mechanisms. We are specialized in cardiorenal & metabolic disease. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI).
Antaros Medical delivers both small, complex, mechanistic studies as well as large, streamlined multi-center clinical trials utilizing our innovative imaging methods. Our global headquarters and analysis Corelab are based in Sweden. If you want to find out more about our company, please go to our website: www.antarosmedical.com.
Our culture is our people, and our values make us everything that we are. Please feel free to have a look upon our Culture Handbook to get to know us even better: Our culture – Antaros Medical. Visa mindre

Are you interested in HR coordination, administration, and assistance within a dynamic work environment? Would you like to work at an innovative company in the global Life Science sector, supporting recruitment and various HR processes? If you're a dedicated student who enjoys working in a structured manner and values teamwork, then you should continue reading.
At Antaros Medical, we prioritize competence, development, ideas, and solutions. Building strong relationships and maintaining trust are key to our success, just as much as having fun while doing a meaningful job. With approximately 130 employees across our offices in Mölndal, Uppsala, and Lund in Sweden, as well as in the US, our team is continuously expanding. As part of our growth journey, we are seeking a part-time HR Assistant to provide HR and recruitment administrative support.
We believe that robust HR processes are crucial for a thriving work environment, which includes recruiting and retaining our great staff. As a part-time HR Assistant, you will join our HR team, assisting with administration, documentation, and general support across various HR processes. You will also help coordinate recruitment and onboarding processes in collaboration with managers and other departments. The position is based at our Mölndal office, and you will be reporting to the VP, HR.
Your main responsibilities will include:
Providing general HR administrative support and assistance.
Managing various HR documentation.
Supporting our recruitment and onboarding processes.
Coordinating organizational engagement activities.

Who are we looking for? We are searching for someone currently studying HR or a related field at the university level, with at least one year left before graduation. You may have some initial experience in HR-related service, administration, and/or recruitment.
As an individual, you should excel in communication and interaction with others, enjoying producing results through support and collaboration. We also value strong administrative skills, an analytical and proactive mindset, and the ability to work in a broad HR setting, which requires a structured approach as well as flexibility and an understanding of the bigger picture.
Since we are committed to learning, development, and growth, we hope you will demonstrate a growth mindset, continually learning and building on both external and internal ideas, while keeping up with the latest news within the HR area. We want you to grow with us!
Requirements:
Current B.Sc. or M.Sc. studies in HR or equivalent.
Fluent English language skills in speech and writing.
At least 1 year of experience within recruitment

Are you interested? We would love to hear from you! Please submit your application through our recruitment system, Teamtailor, including your CV, no later than April 11, 2025. We will contact and interview candidates continuously throughout the recruitment process.
For more information about the position, please contact Sofia Löwstedt, VP HR, at [email protected].
This position is for part-time employment, corresponding to approx. 2 days per week, depending on our needs and your availability.

About Antaros Medical At Antaros Medical, we combine ground-breaking imaging with profound experience in drug development and deep knowledge of disease mechanisms. We are specialized in cardiorenal & metabolic disease. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI).
Antaros Medical delivers both small, complex, mechanistic studies as well as large, streamlined multi-center clinical trials utilizing our innovative imaging methods. Our global headquarters and analysis Corelab are based in Sweden. If you want to find out more about our company, please go to our website: www.antarosmedical.com.
Our culture is our people, and our values make us everything that we are. Please feel free to have a look upon our Culture Handbook to get to know us even better: Our culture – Antaros Medical. Visa mindre

Do you find it exciting to work with IT-systems and system administration, as well as being involved and lead various IT-related projects? Would you like to work as a System Administrator in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? Do you enjoy reaching goals in a fast-paced environment through teamwork and collaboration? If this ticks your boxes, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development.

We value competence and development as well as ideas and solutions. Relations and trust are keys to success, and it is equally important for us to have fun while doing a meaningful job. We currently have around 130 employees working at our offices in Sweden in Gothenburg, Uppsala and Malmö, as well as a newly established subsidiary in the US, and we are continuously growing and developing.


As a part of our growth journey, we are looking for a System Administrator for system management. The position will ideally be positioned at our office in Uppsala or Gothenburg.

As a System Administrator, you will handle internal systems including Office 365, Azure Active Directory, hosted systems and cloud applications. You will be responsible for our system life cycle management process and be part of IT-related projects supporting the company's digitization and expansion.


Your main responsibilities will be:


- System life cycle management

- Initiate and implement system and process improvements as well as run and participate in IT system and IT security-related projects

- System implementation, patch management, security management

- IT and system related support


Additional responsibilities could include:

- IT system-training of internal staff


Who are we looking for?

We believe that you have gained initial technical skills from education and/or from work experience including system management, administration, and development. You can work both independently as well as interact with others in a supportive IT-function.

As a person, you are service-minded and have an analytical ability to approach and solve IT-related problems of a different character, by being proactive and taking own responsibility. You have further a clear sense of details and enjoy working with focus and structure.


Requirements:

- At least 2 years work experience of system administration, system development, and/or IT help desk

- Proficiency in Azure AD/Office365 and Powershell

- Solid knowledge of PC/Windows environment

- Proficiency in IT and Information Security practices

It is perceived as beneficial if you have post-secondary education of IT, for instance, in applied systems science, or hold an equivalent education from a related field.


Meritorious:

It is further meritorious if you have experience in network equipment (Fortinet, HP), database management, public clouds, system requirements management, validation and testing.

In addition, we perceive it as an advantage if you have work experience from the medical industry, with knowledge of ISO27001, GAMP, and ITIL.


Are you interested?

We are happy to hear! Please submit your application via this link with a short personal letter (in English) and your CV included, no later than October 15th, 2023. Interviews are held continuously during the advertisement period.

For more information about the position, please contact Johannes Carlsson, VP IT, +46 73 917 86 50.

The recruitment is for permanent employment.

We only accept applications via our recruitment system, Teamtailor. The recruitment is handled by Antaros Medical.



About Antaros Medical

At Antaros Medical, we combine ground-breaking imaging with profound experience in drug development and deep knowledge of disease mechanisms. We are specialized in cardiorenal & metabolic diseases and oncology. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI) and COST.

Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden, and we have recently opened a subsidiary in the US. If you want to find out more about our company, go to our website: www.antarosmedical.com (https://antarosmedical.com/) Visa mindre

Tycker du det är spännande att arbeta med IT-system och systemadministration, utveckling, samt att vara med och leda olika IT-relaterade projekt? Skulle du vilja arbeta som Systemadministratör i ett växande företag som ägnar sig åt att göra verklig skillnad i läkemedelsutveckling genom banbrytande bildbehandling? En plats som ständigt går framåt, med fantastisk vetenskap, fantastiska människor och en informell atmosfär? Gillar du att nå mål i en fartfylld miljö genom teamwork och samarbete? Om detta stämmer in på dig, bör du fortsätta läsa.

På Antaros Medical är vi banbrytande inom bildbehandlingsmetoder, såsom Magnetisk Resonanstomografi (MRI) och Positron Emission Tomography (PET), för att designa och leverera kliniska studier för beslutsfattande och differentiering i läkemedelsutveckling.

Vi värdesätter såväl kompetens och utveckling som idéer och lösningar. Relationer och förtroende är nycklarna till framgång, och det är lika viktigt för oss att ha roligt samtidigt som vi gör ett meningsfullt jobb. Vi har idag cirka 130 anställda på våra kontor i Sverige i Göteborg, Uppsala och Malmö, samt ett nyetablerat dotterbolag i USA, och vi växer och utvecklas kontinuerligt.

Som en del av vår tillväxtresa söker vi en Systemadministratör.
Tjänsten kommer att vara placerad på vårt kontor i Uppsala eller Göteborg.

Som systemadministratör kommer du att hantera interna system inklusive Office 365, Azure Active Directory, SaaS-lösningar och Cloudapplikationer. Du kommer att ansvara för livscykelhantering och utveckling av system och ingå i IT-relaterade projekt som stödjer företagets digitalisering och expansion.

Dina huvudsakliga ansvarsområden kommer vara:

- Livscykelhantering av system

- Initiera, utveckla och implementera system- och processförbättringar samt driva och delta i projekt som rör IT-system och IT-säkerhet.

- Systemuppsättning, patchhantering, säkerhetshantering

- IT- och systemsupport

Ytterligare ansvarsområden kan inkludera:

- IT-och systemutbildning av intern personal

Vem letar vi efter?

Vi tror att du har har tekniska färdigheter från utbildning och/eller från arbetslivserfarenhet inklusive systemdrift, administration och utveckling. Du kan arbeta både självständigt och interagera med andra i en stödjande IT-funktion.

Som person är du serviceinriktad och har en analytisk förmåga att närma dig och lösa IT-relaterade problem, genom att vara proaktiv och ta eget ansvar. Du har vidare en tydlig känsla för detaljer och trivs med att arbeta med fokus och struktur.

Utbildning och erfarenhet:

- Minst 2 års arbetslivserfarenhet inom systemadministration, systemutveckling och/eller IT help desk.

- Kunskaper i Azure AD/Office365 och Powershell

- Gedigna kunskaper om PC/Windows-miljö

- Flytande engelska i tal och skrift

- God kännedom om arbete med IT och Informationssäkerhet.

Det är meriterande om du har eftergymnasial utbildning inom IT, till exempel inom systemvetenskap, eller har motsvarande utbildning från ett närliggande område.



Meriterande:

Arbetslivserfarenhet av systemadministration, systemutveckling och/eller IT helpdesk.

Det är vidare meriterande om du har erfarenhet av nätverksutrustning (Fortinet, HP), databashantering, publika moln, systemkravshantering, systemvalidering, loggranskning och testning och/eller mjukvaruutveckling inom MS DevOps.

Dessutom ser vi det som meriterande om du har arbetslivserfarenhet från läkemedelsbranschen, med kunskap om ISO27001, GAMP, och ITIL.



Är du intresserad?

Skicka in din ansökan via denna länk med ett kort personligt brev (på engelska) och ditt CV, senast den 15:e Oktober, 2023. Vi håller i intervjuer löpande.

För mer information om tjänsten, vänligen kontakta Johannes Carlsson, VP IT, +46 73 917 86 50, eller [email protected] (https://app.teamtailor.com/companies/wQQWuM-jFpM/jobs/2064136/edit/[email protected]).

Rekryteringen avser en tillsvidareanställning.

Vi tar endast emot ansökningar via vårt rekryteringssystem, Teamtailor. Rekryteringen sköts av Antaros Medical. Kontakt från rekryterare undanbedes.

Om Antaros Medical

På Antaros Medical kombinerar vi banbrytande bildbehandling med djup erfarenhet av läkemedelsutveckling och djup kunskap om sjukdomsmekanismer. Vi är specialiserade på kardiorenala och metabola sjukdomar och onkologi. Vi har ett globalt nätverk av partner och kunder, inklusive både Big Pharma och Biotechs, och flera europeiska samarbetsinitiativ som Innovative Medicines Initiative (IMI) och COST.

Antaros Medical har levererat små komplexa, mekanistiska studier såväl som multicenterstudier i kliniska prövningar över hela världen med hjälp av våra innovativa avbildningsmetoder. Vårt globala huvudkontor och Imaging Corelab är baserat i Sverige, och vi har nyligen öppnat ett dotterbolag i USA. Om du vill veta mer om vårt företag, gå till vår hemsida: www.antarosmedical.com (https://antarosmedical.com/). Kulturen är våra människor och våra värdeord utgör allting som vi gör. Ta gärna en titt på vår kulturhandbok för att lära känna oss ännu mer: Our culture - Antaros Medical (https://antarosmedical.com/our-culture/). Visa mindre

Would you like to work as an MR Imaging Specialist in a growing company devoted to making a real difference in drug development through ground-breaking imaging? Do you highlight communication skills, collaboration, and the importance of quality in your work? How about working in place that is constantly moving forward, with great science, great people, and an informal atmosphere? If this ticks your boxes, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development. We currently have around 120 employees working at our offices in Sweden in Gothenburg, Uppsala and Malmö, as well as a newly established subsidiary in the US, and we are continuously growing and developing. ´

As a part of our growth journey, we are now looking for an MR Imaging Specialist. The position will be placed in either our Gothenburg, Uppsala, or Malmö office.

As an MR Imaging Specialist, you will be involved in the start-up and operational phase of clinical trials to ensure the best quality of MR images collected on the clinical imaging sites and by participating in our contract research studies and as part of our own R&D. Your main focus will be the responsibility for setting up harmonized imaging protocols, training the sites on the procedures, and communicating with imaging site staff.

You will join a group of Imaging Specialists with expertise in MR and PET, and you will be working closely with Imaging Scientists, Project Managers, and Image Analysts to deliver innovative imaging solutions to the pharmaceutical industry.

Your main responsibilities will be:

- Assuring image quality and managing imaging aspects of clinical trials

- On-site and remote training, assessment and qualifying of imaging sites

- Supporting imaging sites with the setting up of imaging protocols according to study requirements

- Educating imaging sites on the processes to be followed in the clinical trials

Who are we looking for?

We believe that you have strong organizational skills, a distinct sense of empowerment, and carry out as well as lead your work independently. Even so, you very much enjoy working in project teams from start to finish to achieve the goal. You are comfortable communicating on the phone, via Teams and per e-mail.

As a person, we further believe that you are outgoing, a natural communicator, and can adapt your approach depending on the situation. You work as a team player and apply communicative and interactive skills on different levels within the organization and with external parties and customers.

Requirements:

- A radiographer’s degree, specialization in MRI

- Clinical MRI-experience working as a radiographer or similar experience

- Experience in working with MRI scanners from multiple vendors

- Strong communication skills in English (written and oral)

Preferably, you have professional experience in abdominal and kidney imaging. It is further beneficial if you have work experience in pharmaceutical- or medical technology industries, and/or experience of working according to GCP and in clinical trials.

Are you interested?

Great to hear! Please submit your application via this link with a short personal letter and your CV included, no later than April 17th, 2023. We will contact and interview candidates continuously throughout the recruitment process.

Please attach degree certificates from higher level education(s) together with your application.

For more information about the position, please contact Nima Tofighi, Manager Imaging Specialists, at [email protected] or +46 (0)76 111 42 47 .

About Antaros Medical

At Antaros Medical, we combine ground-breaking imaging with profound experience in drug development and deep knowledge of disease mechanisms. We are specialised in cardiorenal & metabolic diseases and oncology. We have a global network of collaboration partners and customers, including both Big Pharma and Biotech, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI) and COST.

Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden. If you want to find out more about our company, visit our website: www.antarosmedical.com (http://www.antarosmedical.com/).

Our culture is our people, and our values make us everything that we are. Please feel free to have a look upon our Culture Handbook to get to know us even better: Our culture - Antaros Medical (https://antarosmedical.com/our-culture/). Visa mindre

Would you like to work as a Clinical Project Manager in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? Do you enjoy reaching goals in a fast-paced environment through teamwork and collaboration? If this ticks your boxes, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development.

We value competence and development as well as ideas and solutions. Relations and trust are keys to success, and it is equally important for us to have fun while doing a meaningful job. We have currently around 125 employees working at our offices in Sweden in Gothenburg, Uppsala and Malmö, as well as a newly established subsidiary in the US, and we are continuously growing and developing.

As a part of our growth journey, we are looking for our next Clinical Project Manager with experience in clinical drug development. You will ideally join our office in Mölndal, Uppsala or Malmö in Sweden, and partly be able to work from home.

As a Clinical Project Manager at Antaros Medical, you will be overall responsible and accountable for project management of the imaging part in clinical trials, from initiation to end of assigned projects. Your responsibility includes to ensure the projects are delivered accordingly with timelines, to the agreed budget, with high quality, and per internal and client’s SOPs, ICH/GCP and other regulation.

Your main responsibilities will be:

- Manage multiple projects ranging in size and complexity, from single to multicenter studies

- Act as a primary contact to the client to ensure smooth operations and communication

- Manage the internal trial team to ensure the right input at the right time from different skills within the company

- Present project information at internal and external meetings

- Risk management responsibility and lessons learned for assigned projects

- Manage the project financials in collaboration with the Finance Department and financial follow-up for assigned projects

Who are we looking for?

We believe that you have demonstrated collaboration skills as well as a team-oriented approach to engage with colleagues and clients. You have the flexibility and the ability to handle multiple tasks and projects to meet deadlines while delivering high-quality work in a dynamic environment.

As a person, we further believe that you are outgoing and enthusiastic, a natural communicator, and can adapt your approach depending on the situation. You work as a team player and apply communicative and interactive skills on different levels within the organization and with external parties and customers.

Requirements:

- University degree within the Life Science field

- At least 3 years’ experience from working with clinical trials from start to end of projects, including experience within project management of clinical trials

- Strong understanding of ICH-GCP and other relevant regulations and guidelines in relation to clinical trials

- Understanding of the full drug development process

- Excellent written and verbal communication skills in English

Are you interested?

Great to hear! Please submit your application via this link with a short personal letter and your CV included, no later than February 12th, 2023.

Please attach degree certificates from higher level education(s) together with your application.

For more information about the position, please contact Emilia Larsson, HR department, at +46 73-728 93 43, or [email protected]

We only accept applications via our recruitment system, Teamtailor. The recruitment is handled by Antaros Medical. We kindly decline any contact from recruitment- or staffing firms.

About Antaros Medical

At Antaros Medical, we combine ground-breaking imaging with profound experience in drug development and deep knowledge of disease mechanisms. We are specialised in cardiorenal & metabolic diseases and oncology. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI) and COST.

Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden, and we have recently opened a subsidiary in the US. If you want to find out more about our company, go to our website: www.antarosmedical.com (http://www.antarosmedical.com/)

Our culture is our people, and our values make us everything that we are. Please feel free to have a look upon our Culture Handbook to get to know us even more: Our culture - Antaros Medical (https://antarosmedical.com/our-culture/) Visa mindre

Would you like to work as a Chief Financial Officer in a growing company devoted to making a real difference in drug development through ground-breaking imaging? How about reaching goals together in a fast-paced environment within financial operations? If this sounds interesting, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision-making and differentiation in drug development.

We value competence and development as well as ideas and solutions. Relations and trust are keys to success, and it is equally important for us to have fun while doing a meaningful job. We currently have around 120 employees working at our offices in Sweden in Gothenburg, Uppsala, and Malmö, as well as a newly established subsidiary in the US, and we are continuously growing and developing.

As a part of our growth journey and to deliver on our commitments, we are looking for a Chief Financial Officer to our Finance and Legal department. The position will be placed in our Mölndal or Uppsala office.

The Chief Financial Officer position is accountable for the financial actions of the company, performing effective risk management and planning the organization’s financial strategy. This includes the development of a strategic as well as tactical financial plan and operational strategy. Being accountable for the metrics tied to that strategy, and the ongoing development and monitoring of control systems designed to preserve company assets as well as report accurate financial results. Furthermore, to serve as a key contact with investors to describe, present and negotiate financial deals.

Your main responsibilities will be:

- Assist in formulating the company's future strategy and supporting tactical decisions
- Develop performance measures that support the company's strategic direction
- Formulate, plan, and present figures supporting the need for capital including key stakeholder discussions with financial institutions in Sweden as well as on a global arena.
- Participate in key decisions as a member of the leadership team
- Manage and lead the financial department and its personnel (including accounting and legal)
- Oversee & be accountable for the company's risk management, funding strategies, and relationships with third parties

Who are we looking for?

The right candidate has a good track record in driving a finance function, preferably in a growth environment, and experience from fundraising. To succeed in the role of Chief Financial Officer, you are:

- Business-oriented with commercial acumen
- Analytical mindset and generally strong with numbers
- Ability to challenge established working methods and be “hands-on” when needed
- Strong leadership and communication skills
- Listed company experience advantage


Requirements:

- Documented experience (>5 years) in similar positions
- Experience from working in growth environments
- Prior experience in fundraising
- Excellent written and verbal communication skills in English
- Excellent verbal and written communication and presentation skills
- High level of computer proficiency in Microsoft Word, Excel, and PowerPoint
- Experience from a listed company is an advantage


Meritorious:

It is meritorious to have worked in a scale-up and fast-growing company.

As a person we believe you have the motivation and strive to learn quickly in a fast-paced, changeable, and dynamic environment.

It is further beneficial with experience of working within a pharmaceutical service-oriented business, e.g., in a CRO, however also not a requirement.


Are you interested?

Great to hear! Please submit your application via this link with a short personal letter and your CV included, no later than 31th March 2023.

For more information about the position, please contact:

Director, HR Sofia Löwstedt +46 (0) 70-7158790 or ([email protected])

About Antaros Medical

At Antaros Medical, we combine ground-breaking imaging with profound experience in drug development and deep knowledge of disease mechanisms. We are specialized in cardiorenal & metabolic diseases and oncology. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicine Initiative (IMI) and COST.

Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden, and we have recently opened a subsidiary in the US. If you want to find out more about our company, go to our website: www.antarosmedical.com (http://www.antarosmedical.com/) Visa mindre

Would you like to work as a Clinical Project Manager in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? Do you enjoy reaching goals in a fast-paced environment through teamwork and collaboration? If this ticks your boxes, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development.

We value competence and development as well as ideas and solutions. Relations and trust are keys to success, and it is equally important for us to have fun while doing a meaningful job. We have currently around 120 employees working at our offices in Sweden in Gothenburg, Uppsala and Malmö, as well as a newly established subsidiary in the US, and we are continuously growing and developing.

As a part of our growth journey, we are looking for our next Clinical Project Manager with experience in clinical drug development. You will ideally join our office in Mölndal, Uppsala or Malmö in Sweden, and partly be able to work from home.

As a Clinical Project Manager at Antaros Medical, you will be overall responsible and accountable for project management of the imaging part in clinical trials, from initiation to end of assigned projects. Your responsibility includes to ensure the projects are delivered accordingly with timelines, to the agreed budget, with high quality, and per internal and client’s SOPs, ICH/GCP and other regulation.

Your main responsibilities will be:

- Manage multiple projects ranging in size and complexity, from single to multicenter studies

- Act as a primary contact to the client to ensure smooth operations and communication

- Manage the internal trial team to ensure the right input at the right time from different skills within the company

- Present project information at internal and external meetings

- Risk management responsibility and lessons learned for assigned projects

- Manage the project financials in collaboration with the Finance Department and financial follow-up for assigned projects

Who are we looking for?

We believe that you have demonstrated collaboration skills as well as a team-oriented approach to engage with colleagues and clients. You have the flexibility and the ability to handle multiple tasks and projects to meet deadlines while delivering high-quality work in a dynamic environment.

As a person, we further believe that you are outgoing and enthusiastic, a natural communicator, and can adapt your approach depending on the situation. You work as a team player and apply communicative and interactive skills on different levels within the organization and with external parties and customers.

Requirements:

- University degree in Life Science

- At least 3 years’ experience from working with clinical trials from start to end of projects

- Experience within project management of clinical trials is meritorious

- Strong understanding of ICH-GCP and other relevant regulations and guidelines in relation to clinical trials

- Understanding of the full drug development process

- Excellent written and verbal communication skills in English

Are you interested?

Great to hear! Please submit your application via this link with a short personal letter and your CV included, no later than January 15th, 2023.

Please attach degree certificates from higher level education(s) together with your application.

For more information about the position, please contact Emilia Larsson, Junior HR Business Partner, +46 73 728 9343 or [email protected]

We only accept applications via our recruitment system, Teamtailor. The recruitment is handled by Antaros Medical. We kindly decline any contact from recruitment- or staffing firms.

About Antaros Medical

At Antaros Medical, we combine ground-breaking imaging with profound experience in drug development and deep knowledge of disease mechanisms. We are specialised in cardiorenal & metabolic diseases and oncology. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI) and COST.

Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden, and we have recently opened a subsidiary in the US. If you want to find out more about our company, go to our website: www.antarosmedical.com (http://www.antarosmedical.com/)

Our culture is our people, and our values make us everything that we are. Please feel free to have a look upon our Culture Handbook to get to know us even more: Our culture - Antaros Medical (https://antarosmedical.com/our-culture/) Visa mindre

Tycker du det är spännande att arbeta med IT-system och systemadministration, utveckling, samt att vara med och leda olika IT-relaterade projekt? Skulle du vilja arbeta som Systemadministratör i ett växande företag som ägnar sig åt att göra verklig skillnad i läkemedelsutveckling genom banbrytande bildbehandling? En plats som ständigt går framåt, med fantastisk vetenskap, fantastiska människor och en informell atmosfär? Gillar du att nå mål i en fartfylld miljö genom teamwork och samarbete? Om detta stämmer in på dig, bör du fortsätta läsa.

På Antaros Medical är vi banbrytande inom bildbehandlingsmetoder, såsom Magnetisk Resonanstomografi (MRI) och Positron Emission Tomography (PET), för att designa och leverera kliniska studier för beslutsfattande och differentiering i läkemedelsutveckling.

Vi värdesätter såväl kompetens och utveckling som idéer och lösningar. Relationer och förtroende är nycklarna till framgång, och det är lika viktigt för oss att ha roligt samtidigt som vi gör ett meningsfullt jobb. Vi har idag cirka 120 anställda på våra kontor i Sverige i Göteborg, Uppsala och Malmö, samt ett nyetablerat dotterbolag i USA, och vi växer och utvecklas kontinuerligt.

Som en del av vår tillväxtresa söker vi en Systemadministratör.
Tjänsten kommer att vara placerad på vårt kontor i Uppsala eller Göteborg. Den här annonsen är för vårt kontor i Göteborg, Mölndal.

Som systemadministratör kommer du att hantera interna system inklusive Office 365, Azure Active Directory, SaaS-lösningar och Cloudapplikationer. Du kommer att ansvara för livscykelhantering och utveckling av system och ingå i IT-relaterade projekt som stödjer företagets digitalisering och expansion.

Dina huvudsakliga ansvarsområden kommer vara:

- Livscykelhantering av system
- Systemuppsättning, patchhantering, säkerhetshantering
- Initiera, utveckla och implementera system- och processförbättringar
- Driva och delta i IT-system och IT-säkerhetsrelaterade projekt
- IT- och systemsupport


Ytterligare ansvarsområden kan inkludera:

- IT-och systemutbildning av intern personal


Vem letar vi efter?

Vi tror att du har har tekniska färdigheter från utbildning och/eller från arbetslivserfarenhet inklusive systemdrift, administration och utveckling. Du kan arbeta både självständigt och interagera med andra i en stödjande IT-funktion.

Som person är du serviceinriktad och har en analytisk förmåga att närma dig och lösa IT-relaterade problem, genom att vara proaktiv och ta eget ansvar. Du har vidare en tydlig känsla för detaljer och trivs med att arbeta med fokus och struktur.

Utbildning och erfarenhet:

- Kunskaper i Azure AD/Office365 och Powershell
- Gedigna kunskaper om PC/Windows-miljö


Det är meriterande om du har eftergymnasial utbildning inom IT, till exempel inom systemvetenskap, eller har motsvarande utbildning från ett närliggande område.

Meriterande:

Arbetslivserfarenhet av systemadministration, systemutveckling och/eller IT helpdesk

Det är vidare meriterande om du har erfarenhet av nätverksutrustning (Fortinet, HP), databashantering, publika moln, systemkravshantering, systemvalidering, loggranskning och testning och/eller mjukvaruutveckling inom MS DevOps.

Dessutom ser vi det som meriterande om du har arbetslivserfarenhet från läkemedelsbranschen, med kunskap om ISO27001, GAMP, och ITIL.



Är du intresserad?

Skicka in din ansökan via denna länk med ett kort personligt brev (på engelska) och ditt CV, senast den 30 oktober 2022.

För mer information om tjänsten, vänligen kontakta Johannes Carlsson, VP IT & QA, +46 73 917 86 50, eller [email protected].

Rekryteringen avser tillsvidareanställning.

Vi tar endast emot ansökningar via vårt rekryteringssystem, Teamtailor. Rekryteringen sköts av Antaros Medical. Kontakt från rekryterare undanbedes.

Om Antaros Medical

På Antaros Medical kombinerar vi banbrytande bildbehandling med djup erfarenhet av läkemedelsutveckling och djup kunskap om sjukdomsmekanismer. Vi är specialiserade på kardiorenala och metabola sjukdomar och onkologi. Vi har ett globalt nätverk av partner och kunder, inklusive både Big Pharma och Biotechs, och flera europeiska samarbetsinitiativ som Innovative Medicines Initiative (IMI) och COST.

Antaros Medical har levererat små komplexa, mekanistiska studier såväl som multicenterstudier i kliniska prövningar över hela världen med hjälp av våra innovativa avbildningsmetoder. Vårt globala huvudkontor och Imaging Corelab är baserat i Sverige, och vi har nyligen öppnat ett dotterbolag i USA. Om du vill veta mer om vårt företag, gå till vår hemsida: www.antarosmedical.com (https://antarosmedical.com/). Där hittar du även vår Kulturhandbok, skapad för att ge dig en inblick i vår kultur och dagliga arbetsliv: Our culture - Antaros Medical (https://antarosmedical.com/our-culture/). Visa mindre

How does working as a QA Specialist in a growing company devoted to making a real difference in drug development through ground-breaking imaging, sound to you? Do you get energy from working in a dynamic environment where you quickly can apply your competence and have a clear impact in your work? How about a place that is constantly moving forward, with great science, great people, and an informal atmosphere? If this catches your interest, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development.

We value competence and development as well as ideas and solutions. Relations and trust are keys to success, and it is equally important for us to have fun while doing a meaningful job. We have currently around 120 employees working at our offices in Sweden in Gothenburg, Uppsala and Malmö, as well as a newly established subsidiary in the US, and we are continuously growing and developing.

To deliver on our commitments, we are now looking for a QA Specialist with experience in clinical drug development and GCP to join us. The position is ideally based in our Uppsala, Mölndal or Malmö office in Sweden but could possibly be placed home-based in Sweden as well, in which case regular travel to our Uppsala or Mölndal office would be expected.

What would you be responsible for as a QA Specialist at Antaros Medical?

As a QA Specialist, you will be working with, and take operationally responsibility for, a large scope of various QA activities and processes within Antaros Medical, including support with improvement and development initiatives within QA.

Your main responsibilities:

- Support the development of new SOPs, templates, and other quality system documents
- Conduct and work with the implementation of internal and external audits
- Host and manage inspections, Sponsor audits, and desk-top audits until closure
- Assist with information in RFIs/vendor assessments
- Work with complaints, deviations and CAPA workflows
- Perform vendor qualification activities
- Provide day to day general QA support internally
- Be up to date with all regulations relevant to our business and inform the organisation of updates


Who are we looking for?

We believe that you are a structured and communicative person who will thrive in our dynamic and rapidly developing environment. You are focused on delivering thorough and high-quality results and enjoy giving quality-related advice to the organisation. You have further a lens for improvement possibilities where initiatives based on your competence and knowledge falls naturally for you in your performance.

You collaborate very well with others, by being attentive and having a team-oriented approach when engaging with colleagues and clients. Last but not least, you value having fun while doing a meaningful job.

Requirements:

- University degree in Natural Science, Medicine or similar field.
- QA-experience in the pharmaceutical industry
- Experience from working with clinical trials
- Understanding of ICH-GCP and other relevant guidelines
- Excellent knowledge of spoken and written Swedish and English


Knowledge within imaging in clinical trials is perceived as an advantage for the role however not required, as well is knowledge in GLP, GMP and/or GDP.

Are you interested?

Wonderful to hear! Please submit your application via the link with a short personal letter (in English) and your CV included, no later than November 27th, 2022.

Please attach degree certificates from higher level education(s) together with your application.

For more information about the position, please contact Johannes Carlsson, VP IT & QA, on +46(0)73-917 86 50, or [email protected]

We only accept applications via our recruitment system, Teamtailor. The recruitment is handled by Antaros Medical. We kindly decline any contact from recruitment- or staffing firms.

About Antaros Medical

At Antaros Medical, we combine ground-breaking imaging with profound experience in drug development and deep knowledge of disease mechanisms. We are specialised in cardiorenal & metabolic diseases and oncology. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI) and COST.

Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden, and we have recently opened a subsidiary in the US.

You are very welcomed to visit our website to learn more about our company: www.antarosmedical.com (http://www.antarosmedical.com)

Our culture is our people, and our values make us everything that we are. Please feel free to have a look upon our Culture Handbook to get to know us even more: Our people - Antaros Medical (https://antarosmedical.com/our-people/) Visa mindre

Would you like to work as a Manager, Imaging Site Management, in a growing company devoted to making a real difference in drug development through ground-breaking imaging? Do you characterize yourself by having a natural drive and interest for process development and shaping new ways of working? How about a managerial responsibility with focus on people, well-being and performance? If this ticks your boxes, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development. We currently have around 120 employees working at our offices in Sweden in Gothenburg, Uppsala and Malmö, as well as a newly established subsidiary in the US, and we are continuously growing and developing.

As a part of our growth journey, we are now looking for a Manager, Imaging Site Management on 50 % employment rate - an exciting leadership position at Antaros Medical. The position could be based in our offices either in Gothenburg, Uppsala or Malmö.

As a Manager, Imaging Site Management, you will have personnel responsibility over the Imaging Specialists, which includes overall responsibility as line manager and resource planning, and further developing the Imaging Specialist role within the company. You will work closely together with Head of Imaging Science, by having great impact of designing and creating the meaning and significance of this managerial role as it will unfold by time, and by working jointly with process development and streamlining of operations within the department of Imaging Science.

Your responsibility will include each step of growing the team of Imaging Specialists, such as actively working with recruitment and onboarding processes.

Your main responsibilities will be:

- To take ownership of the build-up and develop the role of Manager, Imaging Site Management, within Imaging Science department
- Further develop the role of the Imaging Specialists at Antaros Medical
- Provide leadership and direction to the Imaging Specialists including mentoring, evaluating performance, coaching, and development of the employees
- Resource planning and allocation of work for employees within the team
- Provide employees in the team with guidance and support with priorities as needed
- Shape and ensure streamlined imaging site management and operations within the team
- Develop and execute short-term and long-term strategies for Imaging Site Management together with Head of Imaging Science


Additional responsibilities could include:

- Co-pilot together with Head of Imaging Science for process development in Imaging Science, including to optimize routines and by addressing challenges and changes
- Recruitment, introduction, and training of newly hired Imaging Specialists


Who are we looking for?

We believe that you are organized and clear-minded as a person, with an energetic yet rational approach to your work. You have the natural drive and interest for improvement and enjoy the everyday challenges as well as pursuing set goals independently and with others.

Analytical skills are a natural part in how you navigate your role, with the ability to take in both the larger perspective and to have the eye for important details. A practical example of that would be to manage breaking down processes for analysis and understanding, and to put them back together again for improvement actions.

We further believe that you are a people person with interpersonal skills, with equal focus on the team as on the individual’s wellbeing and performance. The managerial ability to tune in on your employees, in different parts of Sweden and in the world, is prioritized for this role.

Requirements:

- A higher education degree such as B. Sc. or M. Sc. in Life Science field, such as radiographer’s degree or equivalent in relevant area
- Extensive professional experience within imaging, where working as an Imaging Specialist or Imaging Director is preferred
- Strong communication skills in English (written and oral)


It is beneficial with work experience in pharmaceutical- or medical technology industries, as well as experience of working according to GCP and in clinical trials. You have preferably experience of having team leader- or managerial responsibilities.

Are you interested?

Great to hear! Please submit your application via this link with a short personal letter and your CV included, no later than 12th June, 2022. We will contact candidates ongoing throughout the process.

For more information about the position, please contact Kerstin Heurling, Head of Imaging Science, at [email protected] or +46 72 233 86 34.

About Antaros Medical

At Antaros Medical, we combine ground-breaking imaging with profound experience in drug development and deep knowledge of disease mechanisms. We are specialised in cardiorenal & metabolic diseases and oncology. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI) and COST.

Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden. If you want to find out more about our company, go to our website: www.antarosmedical.com (http://www.antarosmedical.com/). Visa mindre

Are you passionate about story-telling and see the beauty in making complex science&solutions; into clear customer focused communication? Would you thrive in a fast-growing environment with lots of opportunities to make a difference? Would you like to work as a Communication Manager in a company that is constantly moving forward, with great science, great people, and an informal atmosphere. If this ticks your boxes, you should continue reading.

At Antaros Medical, we develop and tailor imaging solutions to help pharmaceutical companies cross the world to understand how drugs work on human pathophysiology - to facilitate decision making for pharmaceutical companies. And in the end get the right medicines as fast as possible to the market

We value competence and development as well as ideas and creativity. Relations and trust are keys to success, and it is equally important for us to have fun while doing a meaningful job. We have currently over 100 employees working at our offices in Sweden in Mölndal, Uppsala and Malmö, as well as a newly established subsidiary in the US, and we are continuously growing and developing.

We are looking for a Communication Manager for a 1-year maternity leave cover, potentially with future possibilities as we are growing our function. You will be part of the Marketing team and support our journey to strengthen our brand awareness globally and to increase sales.

Depending on your level of experience, your main responsibilities will be to:

- Drive and execute content generation and communication fit for different channels including social media (mainly LinkedIn). This includes brand awareness campaigns, news, press releases, articles, case studies, employer branding stories etc.

- Work closely with different internal functions including sales, R&D, clinical operations, and other relevant stakeholders in both strategy development and hands-on executions making complex science and solutions into clear customer focused communication.
- Support VP, Strategy and Marketing, in continuing to develop and implement marketing&communication; strategies and plans. This also includes specific business area/disease area communication objectives


- Keep our website updated

- Managing different brand&communication; agencies

- Manage customer insights and monitor&evaluate; results of marketing&communication; actions

Ideally, this position will be placed in our Gothenburg office.

What about you?

We believe you enjoy a growth journey and are looking for a passionate, dynamic and collaborate environment. You are a highly pro-active and solution-oriented person with versatility to shift from strategic level to "hands on" execution. You are comfortable in building, driving, and implementing communication strategies and campaigns driving brand awareness and willingness to act including making difficult science into clear customer focused communication.

We believe you have:

- A university degree from relevant area eg Marketing, Communication, Journalism or Life science

- Proven experience in a communication manager role or similar

- Proven track record of establishing positive relationships, both internally and externally

- Excellent written and spoken communication skills in English

- Proven digital experience through web and across social media, specifically LinkedIn

Experience from the Medtech/Life-science industry is perceived as beneficial for the role. where knowledge of drug development as a further advantage. PR experience is also a plus.

Are you interested?

Great to hear! Please submit your application via this link with a short personal letter and your CV included, no later than May 30th, 2022.

The above are not hard requirements! If you have a different profile but you see that you have relevant skills and you think you can do a remarkable job, apply, and share with us your motivation on why we should meet you.

For more information about the position, please contact Christina Moberg, +46 (0)708-467041, or [email protected].

About Antaros Medical

At Antaros Medical, we combine ground-breaking imaging with profound experience in drug development and deep knowledge of disease mechanisms. We are specialized in cardiorenal & metabolic diseases and oncology. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI) and COST.

Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden, and we have recently opened a subsidiary in the US. If you want to find out more about our company, go to our website: www.antarosmedical.com (https://antarosmedical.com/) Visa mindre

Are you interested in project coordination in clinical trials? Would you like to work in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? If this catches your interest, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development.

We value competence and development as well as ideas and solutions. Relations and trust are keys to success, and it is equally important for us to have fun while doing a meaningful job. We have currently over 100 employees working at our offices in Sweden in Gothenburg, Uppsala and Malmö, as well as a newly established subsidiary in the US.

To deliver on our commitments, we are looking for our next Clinical Trial Coordinator, with experience in clinical drug development and project coordination. As a Clinical Trial Coordinator, you will be responsible for coordination in and administration of our clinical trials. The position will be located in our office in Gothenburg.

Your main responsibilities will be:

- Provide general administrative support and assistance to the internal project team, primarily the Project Manager.
- Support the internal project team with ongoing conduct of studies including coordination of administrative tasks during the study process
- Contribute to applications & submissions by handling clinical-regulatory documents
- Assist in contact with clinical sites for specific requests (e.g., enrollment updates, missing documentation, meeting arrangements)
- Attend project team meetings and generate meeting minutes
- Set up, organize, and maintain clinical study documentation in the trial master file
- Quality control of and archival of the TMF after final study
- Collaboration with third-party archive vendor


Who are we looking for?

We believe that you have demonstrated collaboration skills as well as a team-oriented approach to engage with colleagues and clients. You have proven administrative skills to handle and structure multiple tasks and projects, in order to meet deadlines in a dynamic environment.

As a person, you are a team player and enjoy interacting with a variety of people in the organization, where you contribute with energy, competence, and ideas.

Requirements:

- Experience from working with clinical trials and according to ICH-GCP
- Level of education that supports skills and capabilities of the position and ensures successful conduct of responsibilities
- Excellent knowledge of spoken and written Swedish and English


Are you interested?

Great to hear! Please submit your application via this link with a short personal letter and your CV included, no later than 22nd May 2022.

For more information about the position, please contact Marie Saether, +46 76 111 06 53, or [email protected].

About Antaros Medical

At Antaros Medical, we combine ground-breaking imaging with profound experience in drug development and deep knowledge of disease mechanisms. We are specialized in cardiorenal & metabolic diseases and oncology. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI) and COST.

Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden, and we have recently opened a subsidiary in the US. If you want to find out more about our company, go to our website: www.antarosmedical.com (http://www.antarosmedical.com/) Visa mindre

Would you like to work with IT and Computerised Systems as a Quality & Compliance Manager, in a growing company devoted to make a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? If this sounds interesting, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development. We are specialized in cardiometabolic diseases (including NAFLD/NASH and chronic kidney disease) and oncology. We have established ourselves as a strategic development partner to the pharmaceutical industry. We combine ground-breaking imaging with profound experience in drug development and deep knowledge of disease mechanisms. Our projects cover clinical trials in all stages of drug development, and we work both with small biotech companies and global big pharma companies. We currently have around 100 employees working at our offices in Mölndal, Uppsala and Malmö.

As Quality & Compliance Manager in IT/Computerised Systems, you will provide QA oversight and support the implementation, development,risk management, validation, management and use of compliance related electronic systems within the business and in the clinical studies in accordance with ICH-GCP, EU/Annex 11, GAMP and FDA/21 CFR part 11, and Data Integrity GxP requirements.

You will also support the internal departments in developing and maintaining SOPs related to electronic systems as well as work with validation, vendor qualification and compliance. You will be working closely with our QA team; VP IT & QA, COO and Head of Software. The position can be based in either Uppsala, Mölndal or Malmö.

As Quality & Compliance Manager in IT/Computerised Systems at Antaros Medical, your main responsibilities will be:

- Ensure that computerized systems are implemented, developed, validated and managed in accordance with the defined processes, SOPs, standards and policies
- Review and approve documents and solutions based on defined processes, SOPs, standards and policies for computerised systemsSupport the development of new and update of existing SOPs, templates and other quality system documents for computerised systems
- Assist in inspections and customer audits and with information in RFIs/vendor assessments
- Advice organisation in data integrity and computerised system related questions concerning compliance with defined SOPs, standards and policies
- Lead and support vendor assessment, qualification and risk-based re-assessment of vendors delivering computerised systems/software
- Take part in validation and release of systems as per internal processes
- Take part in validation of data lifecycle in clinical studies
- Take part in changes of systems as per internal processes
- Perform activities related to the maintenance of the validated state for computerised systems as per internal processes
- Support the clinical study teams in questions related to computerized systems and data integrity/data lifecycles in specific studies
- Lead and provide support for CAPAs, issues and system non-conformities for computerised systems
- Identify suggestions for improvements and lead improvement projects related to processes, SOPs, standards and policies for computerised systems


Who you are

We believe that you are a structured and communicative person who will thrive in our dynamic and rapidly developing environment. You are focused on delivering high-quality results and enjoy giving quality related advice to the organisation. You collaborate very well with others and have a team-oriented approach when engaging with colleagues and clients. Last but not least, you value having fun while doing a meaningful job.

Requirements

- University degree in Natural Science, Engineering/IT or Medicine.
- Experience within the pharmaceutical-, biotech- or medtech industry as an IT Subject Matter Expert, within quality assurance (QA) working with quality or computerised system
- Excellent knowledge of spoken and written English


Meritorious

- Experience from clinical trials from the pharmaceutical-, biotech- or medtech industry, CROs, or similar business
- Understanding of ICH-GCP, EU/Annex 11, GAMP and FDA/21 CFR part 11 and Data Integrity GxP requirements, and other relevant guidelines concerning both operational aspects as well as quality aspects


More information

For more information about the position, please contact Johannes Carlsson, VP IT & QA
46 73 9178650

Please submit your application via this link with a short personal letter in English and your CV included, no later than April 22nd, 2022. Visa mindre

Would you like to work as an MR Imaging Specialist in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? If this ticks your boxes, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development. We currently have around 90 employees working at our offices in Sweden (Mölndal and Uppsala) and we are continuously growing and developing. As a part of our growth journey, we are now looking for an MR Imaging Specialist.

As an MR Imaging Specialist, you will be involved in the start-up and operational phase of clinical trials ensuring the best quality of MR images collected on the clinical imaging sites participating in our contract research studies and as part of our own R&D. Your main focus will be responsibility for setting up harmonized imaging protocols, training the sites on the procedures and communicating with imaging site staff.

You will join a group of imaging specialists with expertise in MR and PET, and you will be working closely with Imaging Scientists, Project Managers, and Image Analysts to deliver innovative imaging solutions to the pharmaceutical industry.

An important aspect of your job will be assuring image quality in clinical studies, including on-site and remote training and assessment of clinical imaging sites. You will be helping the imaging sites with the setting up of imaging protocols according to study requirements and educating them on the processes to be followed in the clinical trials that we work on.

Your main responsibilities will be:

- Managing imaging aspects of clinical trials
- Training and qualifying imaging sites


Requirements:

- A radiographer’s degree, specialization in MRI
- Extensive clinical MRI experience working as a radiographer or similar
- Experience in working with MRI scanners from multiple vendors
- Strong communication skills in English (written and oral)


Preferred qualifications:

- Experience in abdominal imaging
- Experience in working according to GCP and in clinical trials
- Experience in the pharmaceutical or medical technology industries




Who are we looking for?

We believe that you have strong organizational skills and drive your work independently, but enjoy working in project teams from start to finish to achieve the goal. You are comfortable communicating on the phone/Teams and e-mail.

As a person, we further believe that you are outgoing and enthusiastic, a natural communicator, and can adapt your approach depending on the situation. You work as a team player and apply communicative and interactive skills on different levels within the organization and with external parties and customers.

More information

For more information about the position, please contact Kerstin Heurling, Manager, Imaging for Projects and R&D , at [email protected] or +46 70 2848096.

Please submit your application via this link with a short personal letter and your CV included, no later than 6th March, 2022.

The position is ideally based in our Uppsala or Mölndal office in Sweden but could possibly be placed internationally home-based in the US or Europe.

If you want to find out more about our company, go to our website: www.antarosmedical.com (http://www.antarosmedical.com)

About Antaros Medical

At Antaros Medical, we combine ground-breaking imaging with profound experience in drug development and deep knowledge of disease mechanisms. We are specialised in cardiorenal & metabolic diseases and oncology. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI) and COST. Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden. Visa mindre

Are you interested in image analysis in clinical trials? Would you like to work in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? If this catches your interest, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development.

To deliver on our commitments, we are looking for people with both broad and deep experience in clinical drug development as well as project management.

As a Clinical Trial Coordinator, you will be responsible for coordination in and administration of our clinical trials. The position will be located in our office in Gothenburg.

Main responsibilities:

- Provide general administrative support and assistance to the internal project team, primarily the Project Manager.
- Support the internal project team with ongoing conduct of studies including coordination of administrative tasks during the study process
- Contribute to applications & submissions by handling clinical-regulatory documents
- Assist in contact with clinical sites for specific requests (e.g., enrollment updates, missing documentation, meeting arrangements).
- Attend project team meetings and generate meeting minutes.
- Set up, organize, and maintain clinical study documentation in the trial master file
- Quality control of and archival of the TMF after final study
- Collaboration with third-party archive vendor


Requirements:

- Experience from working with clinical trials and according to ICH-GCP
- Level of education that supports skills and capabilities of the position and ensures successful conduct of responsibilities
- Collaboration skills in order to engage with people and clients
- Proven administrative skills
- Excellent knowledge of spoken and written Swedish and English


More information

For more information about the position, please contact Marie Saether, +46 76 111 06 53, or [email protected].

Please submit your application via this link with a short personal letter and your CV included, no later than 6th March 2022. We only accept applications via our recruitment system, Teamtailor. The recruitment is handled by Antaros Medical.

About Antaros Medical
At Antaros Medical, we are specialised in cardiometabolic diseases (including NAFLD/NASH and chronic kidney disease) and oncology. We have established ourselves as a strategic development partner to the pharmaceutical industry, where we combine ground-breaking imaging with profound experience in drug development and deep knowledge in disease mechanisms. Our projects cover clinical trials in all stages of drug development, and we work both with small biotech companies as well as global big pharma companies. We currently have around 90 employees working at our offices in Mölndal and Uppsala. Visa mindre

Would you like to work as an MR Imaging Specialist in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? If this ticks your boxes, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development. We currently have around 90 employees working at our offices in Sweden (Mölndal and Uppsala) and we are continuously growing and developing. As a part of our growth journey, we are now looking for an MR Imaging Specialist.

As an MR Imaging Specialist, you will be involved in the start-up and operational phase of clinical trials ensuring the best quality of MR images collected on the clinical imaging sites participating in our contract research studies and as part of our own R&D. Your main focus will be responsibility for setting up harmonized imaging protocols, training the sites on the procedures and communicating with imaging site staff.

You will join a group of imaging specialists with expertise in MR and PET, and you will be working closely with Imaging Scientists, Project Managers, and Image Analysts to deliver innovative imaging solutions to the pharmaceutical industry.

An important aspect of your job will be assuring image quality in clinical studies, including on-site and remote training and assessment of clinical imaging sites. You will be helping the imaging sites with the setting up of imaging protocols according to study requirements and educating them on the processes to be followed in the clinical trials that we work on.

Your main responsibilities will be:

- Managing imaging aspects of clinical trials
- Training and qualifying imaging sites


Requirements:

- A radiographer’s degree, specialization in MRI
- Extensive clinical MRI experience working as a radiographer or similar
- Experience in working with MRI scanners from multiple vendors
- Strong communication skills in English (written and oral)


Preferred qualifications:

- Experience in abdominal imaging
- Experience in working according to GCP and in clinical trials
- Experience in the pharmaceutical or medical technology industries




Who are we looking for?

We believe that you have strong organizational skills and drive your work independently, but enjoy working in project teams from start to finish to achieve the goal. You are comfortable communicating on the phone/Teams and e-mail.

As a person, we further believe that you are outgoing and enthusiastic, a natural communicator, and can adapt your approach depending on the situation. You work as a team player and apply communicative and interactive skills on different levels within the organization and with external parties and customers.

More information

For more information about the position, please contact Sofia Löwstedt, HR Director, at [email protected] or +46707158790.

Please submit your application via this link with a short personal letter and your CV included, no later than January 20, 2022.

The position is ideally based in our Uppsala or Mölndal office in Sweden but could possibly be placed internationally home-based in the US or Europe.

If you want to find out more about our company, go to our website: www.antarosmedical.com (http://www.antarosmedical.com)

About Antaros Medical

At Antaros Medical, we combine ground-breaking imaging with profound experience in drug development and deep knowledge of disease mechanisms. We are specialised in cardiorenal & metabolic diseases and oncology. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI) and COST. Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden. Visa mindre

Does HR coordination, administration and assistance in a dynamic work environment sound interesting to you? How about working in an innovative company within the global Life Science sector where you support with recruitment and different HR processes? Are you a driven student who enjoys producing results through structure and collaboration? If it catches your interest, you should continue reading.

At Antaros Medical, we value competence and development as well as ideas and creative solutions. Relations and trust are keys to success, and it is equally important for us to have fun while doing a meaningful job. We have currently around 100 employees working at our offices in Sweden in Mölndal and Uppsala, as well as in the US, and we are continuously growing. As a part of our growth journey, we are looking for a part-time HR Administrator for HR- and recruitment administrative support, to join our Mölndal office.

We believe that good HR processes are essential for a thriving work environment, and so is recruiting and retaining our great people. You will be joining our small but wonderful HR team. As an HR Administrator, you will support the HR function with administration, documentation, and general assistance in various HR processes. You will further assist with coordination of recruitment- and on-boarding processes in collaboration with managers and other departments in the organization.

Your main responsibilities will be:

- Provide general HR administrative support and assistance
- Manage various HR documentation
- Support our recruitment- and on-boarding processes


Additional responsibilities could include:

- Coordinate organizational engagement activities

Who are we looking for?

We believe that you are currently studying HR or an equivalent education at university level, having at least 1 year of studies left before graduation. You might have initial experience of working with HR-related service, administration, and/or recruitment.

As a person, you are service-minded and have a good ability to communicate and interact with others, where you enjoy producing results through support and collaboration. We further believe that you have strong administrative skills as well as an analytical and proactive mindset. You will be working in a broad HR setting, which requires a structured mindset as well as flexibility by understanding prioritizations and the bigger picture.

Requirements:

- Current B. Sc. studies within HR or equivalent
- Fluent English language skills in speech and writing


It is perceived as meritorious if you are studying a M. Sc. within HR or equivalent education. It is further beneficial if you have previous experience of HR service, administration, and/or recruitment.

Are you interested?

Happy to hear! Please submit your application via the link below with your CV included, no later than 23rd January 2022.

For more information about the position, please contact Emilia Larsson, [email protected].

The recruitment is for a part-time employment corresponding to 1-2 days per week.

We only accept applications via our recruitment system, Teamtailor. The recruitment is handled by Antaros Medical.



About Antaros Medical

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development. We are specialized in cardiorenal & metabolic diseases and oncology.

We combine ground-breaking imaging with profound experience in drug development and a deep knowledge in disease mechanisms. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI) and COST. Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden, and we have recently opened a subsidiary in the US. Visa mindre

Would you like to work as a Clinical Project Manager in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? Do you enjoy reaching goals in a fast-paced environment through teamwork and collaboration? If this ticks your boxes, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development.

We value competence and development as well as ideas and creativity. Relations and trust are keys to success, and it is equally important for us to have fun while doing a meaningful job. We have currently around 90 employees working at our offices in Sweden in Mölndal and Uppsala, as well as a newly established subsidiary in the US, and we are continuously growing and developing.

As a part of our growth journey, we are looking for our next Clinical Project Manager with experience in clinical drug development. You will ideally join our office in Mölndal or Uppsala in Sweden, with flexibility to partly work home-based. The position could possibly be placed internationally home-based in the US or Europe.

As a Clinical Project Manager at Antaros Medical, you will be overall responsible and accountable for project management of the imaging part in clinical trials, from initiation to end of assigned projects. Your responsibility includes to ensure the projects are delivered accordingly with timelines, to the agreed budget, with high quality, and per internal and client’s SOPs, ICH/GCP and other regulation.

Your main responsibilities will be:

- Manage multiple projects ranging in size and complexity, from single to multicenter studies
- Act as a primary contact to the client to ensure smooth operations and communication
- Manage the internal trial team to ensure the right input at the right time from different skills within the company
- Present project information at internal and external meetings
- Risk management responsibility and lessons learned for assigned projects
- Manage the project financials in collaboration with the Finance Department and financial follow-up for assigned projects


Who are we looking for?

We believe that you have demonstrated collaboration skills as well as a team-oriented approach to engage with colleagues and clients. You have the flexibility and the ability to handle multiple tasks and projects to meet deadlines while delivering high-quality work in a dynamic environment.

As a person, we further believe that you are outgoing and enthusiastic, a natural communicator, and can adapt your approach depending on the situation. You work as a team player and apply communicative and interactive skills on different levels within the organization and with external parties and customers.

Requirements:

- University degree in Life Science
- At least 3 years’ experience from working with clinical trials from start to end of projects
- Experience within project management of clinical trials is meritorious
- Strong understanding of ICH-GCP and other relevant regulations and guidelines in relation to clinical trials
- Understanding of the full drug development process
- Excellent written and verbal communication skills in English


Are you interested?

Great to hear! Please submit your application via this link with a short personal letter and your CV included, no later than November 30th , 2021.

For more information about the position, please contact Neha Mehta, +46 76 111 06 59, or [email protected].

About Antaros Medical

At Antaros Medical, we combine ground-breaking imaging with profound experience in drug development and deep knowledge of disease mechanisms. We are specialised in cardiorenal & metabolic diseases and oncology. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI) and COST.

Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden, and we have recently opened a subsidiary in the US. If you want to find out more about our company, go to our website: www.antarosmedical.com (http://www.antarosmedical.com/) Visa mindre

Would you like to work as a Clinical Project Manager in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? Do you enjoy reaching goals in a fast-paced environment through teamwork and collaboration? If this ticks your boxes, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development.

We value competence and development as well as ideas and creativity. Relations and trust are keys to success, and it is equally important for us to have fun while doing a meaningful job. We have currently around 90 employees working at our offices in Sweden in Mölndal and Uppsala, as well as a newly established subsidiary in the US, and we are continuously growing and developing.

As a part of our growth journey, we are looking for our next Clinical Project Manager with experience in clinical drug development. You will ideally join our office in Mölndal or Uppsala in Sweden, with flexibility to partly work home-based. The position could possibly be placed internationally home-based in the US or Europe.

As a Clinical Project Manager at Antaros Medical, you will be overall responsible and accountable for project management of the imaging part in clinical trials, from initiation to end of assigned projects. Your responsibility includes to ensure the projects are delivered accordingly with timelines, to the agreed budget, with high quality, and per internal and client’s SOPs, ICH/GCP and other regulation.

Your main responsibilities will be:

- Manage multiple projects ranging in size and complexity, from single to multicenter studies
- Act as a primary contact to the client to ensure smooth operations and communication
- Manage the internal trial team to ensure the right input at the right time from different skills within the company
- Present project information at internal and external meetings
- Risk management responsibility and lessons learned for assigned projects
- Manage the project financials in collaboration with the Finance Department and financial follow-up for assigned projects


Who are we looking for?

We believe that you have demonstrated collaboration skills as well as a team-oriented approach to engage with colleagues and clients. You have the flexibility and the ability to handle multiple tasks and projects to meet deadlines while delivering high-quality work in a dynamic environment.

As a person, we further believe that you are outgoing and enthusiastic, a natural communicator, and can adapt your approach depending on the situation. You work as a team player and apply communicative and interactive skills on different levels within the organization and with external parties and customers.

Requirements:

- University degree in Life Science
- At least 3 years’ experience from working with clinical trials from start to end of projects
- Experience within project management of clinical trials is meritorious
- Strong understanding of ICH-GCP and other relevant regulations and guidelines in relation to clinical trials
- Understanding of the full drug development process
- Excellent written and verbal communication skills in Swedish and English


Are you interested?

Great to hear! Please submit your application via this link with a short personal letter and your CV included, no later than 30th September, 2021.

For more information about the position, please contact Neha Mehta, +46 76 111 06 59, or [email protected].

About Antaros Medical

At Antaros Medical, we combine ground-breaking imaging with profound experience in drug development and deep knowledge of disease mechanisms. We are specialised in cardiorenal & metabolic diseases and oncology. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI) and COST.

Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden, and we have recently opened a subsidiary in the US. If you want to find out more about our company, go to our website: www.antarosmedical.com (http://www.antarosmedical.com/) Visa mindre

Are you interested in image analysis in clinical trials? Would you like to work in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? If this catches your interest, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development.

To deliver on our commitments, we are looking for people with both broad and deep experience in clinical drug development as well as project management.

As a Clinical Trial Assistant, you will be responsible for coordination in and administration of our clinical trials. The role may also include overall administrative support in driving our business forward. The position will be located in our office in Uppsala or Mölndal.

Main responsibilities:

- Provide general administrative support and assistance to the internal project team, primarily the Project Manager.
- Support the internal project team with ongoing conduct of studies including coordination of administrative tasks during the study process
- Contribute to applications & submissions by handling clinical-regulatory documents
- Assist in contact with clinical sites for specific requests (e.g., enrollment updates, missing documentation, meeting arrangements).
- Attend project team meetings and generate meeting minutes.
- Set up, organize, and maintain clinical study documentation in the trial master file
- Quality control of and archival of the TMF after final study
- Collaboration with third-party archive vendor
- General company administration, such as travel booking, expenses, presentations, meetings, etc


Requirements:

- Experience from working with clinical trials and according to ICH-GCP
- Level of education that supports skills and capabilities of the position and ensures successful conduct of responsibilities
- Collaboration skills in order to engage with people and clients
- Proven administrative skills
- Excellent knowledge of spoken and written Swedish and English


More information

For more information about the position, please contact Sofia Löwstedt, HR Director, +46 707 15 87 90

Please submit your application via this link with a short personal letter and your CV included, no later than July 4, 2021. We only accept applications via our recruitment system, Teamtailor. The recruitment is handled by Antaros Medical.

About Antaros Medical
At Antaros Medical, we are specialised in cardiometabolic diseases (including NAFLD/NASH and chronic kidney disease) and oncology. We have established ourselves as a strategic development partner to the pharmaceutical industry, where we combine ground-breaking imaging with profound experience in drug development and deep knowledge in disease mechanisms. Our projects cover clinical trials in all stages of drug development, and we work both with small biotech companies as well as global big pharma companies. We currently have around 90 employees working at our offices in Mölndal and Uppsala. Visa mindre

Would you like to work as a QA Director in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? If this catches your interest, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development. We currently have around 90 employees working at our offices in Sweden in Mölndal and Uppsala, and we are continuously growing and developing. To deliver on our commitments, we are now looking for a QA Director with broad and deep experience in clinical drug development and GCP to join us. The position is ideally based in our Uppsala or Mölndal office in Sweden but could possibly be placed home-based in Sweden or Europe, in which case regular travel to our Uppsala or Mölndal office would be expected.

As a QA Director, you will be overall responsible for all QA activities within Antaros Medical. You will ensure Antaros Medical´s quality by conducting necessary audits and training to guarantee that our operations comply and run smoothly and that clinical trials and R&D activities are performed in accordance with applicable study protocols and in compliance with laws, regulations, guidelines, and our processes. You will be working closely with our QA team and you will be reporting to the VP IT & QA.

As QA Director at Antaros Medical, your main responsibilities will be:

- Lead the QA function, together with the VP QA & IT
- Manage and maintain the Quality System in collaboration with all functional leads and other QA colleagues
- Support the development of new SOPs, templates, and other quality system documents and perform gap analysis
- Responsible for developing and maintaining all QA SOPs related to GCP
- Plan, conduct and report internal and external audits as detailed in the risk-based audit plan
- Host and manage inspections, Sponsor audits, and desk-top audits until closure
- Assist with information in RFIs/vendor assessments
- Manage complaints and deviations
- Manage and follow-up on the full CAPA process, including CAPA effectiveness
- Vendor assessment, qualification, and risk-based re-assessment
- Lead and arrange internal training in relevant areas such as GCP, GDPR, Quality system, etc
- Provide day to day general QA support internally
- Be up to date with all regulations relevant to our business and inform the organisation of updates


Who you are

We believe that you are a structured and communicative person who will thrive in our dynamic and rapidly developing environment. You are focused on delivering high-quality results and enjoy giving quality-related advice to the organisation. You collaborate very well with others and have a team-oriented approach when engaging with colleagues and clients. And last but not least, you value having fun while doing a meaningful job.

Requirements:

- University degree in Natural Science or Medicine.
- Several years’ experience from clinical trials from the pharmaceutical industry, CROs, or similar business including several years of experience in a QA position
- Extensive understanding of ICH-GCP and other relevant guidelines in relation to both operational aspects as well as quality aspects
- Broad understanding of the full drug development process
- Thorough understanding of strategic and operational aspects within clinical research and development
- Knowledge within imaging in clinical trials is an advantage
- Excellent knowledge of spoken and written Swedish and English


Are you interested?

We are happy to hear! Please submit your application via this link with a short personal letter (in English) and your CV included, no later than August 22th, 2021.

For more information about the position, please contact Johannes Carlsson, VP IT&QA;, +46 73 917 86 50 or [email protected]

We only accept applications via our recruitment system, Teamtailor. The recruitment is handled by Antaros Medical.

About Antaros Medical

At Antaros Medical, we combine ground-breaking imaging with profound experience in drug development and deep knowledge of disease mechanisms. We are specialised in cardiorenal & metabolic diseases and oncology. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI) and COST. Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden. Visa mindre

Would you like to work as an MR Imaging Specialist in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? If this ticks your boxes, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development. We currently have around 90 employees working at our offices in Sweden (Mölndal and Uppsala) and we are continuously growing and developing. As a part of our growth journey, we are now looking for an MR Imaging Specialist. The role will be based in either Uppsala or Mölndal.

As an MR Imaging Specialist, you will be involved in the start-up and operational phase of clinical trials ensuring the best quality of MR images collected on the clinical imaging sites participating in our contract research studies and as part of our own R&D. Your main focus will be responsibility for setting up harmonized imaging protocols, training the sites on the procedures and communicating with imaging site staff.

You will join a group of imaging specialists with expertise in MR and PET, and you will be working closely with Imaging Scientists, Project Managers, and Image Analysts to deliver innovative imaging solutions to the pharmaceutical industry.

An important aspect of your job will be assuring image quality in clinical studies, including on-site and remote training and assessment of clinical imaging sites. You will be helping the imaging sites with the setting up of imaging protocols according to study requirements and educating them on the processes to be followed in the clinical trials that we work on.

Your main responsibilities will be:

- Managing imaging aspects of clinical trials
- Training and qualifying imaging sites


Requirements:

- A radiographer’s degree, specialization in MRI
- Extensive clinical MRI experience working as a radiographer or similar
- Experience in working with MRI scanners from multiple vendors
- Strong communication skills in English (written and oral)


Preferred qualifications:

- Experience in abdominal imaging
- Experience in working according to GCP and in clinical trials
- Experience in the pharmaceutical or medical technology industries


Who are we looking for?

We believe that you have strong organizational skills and drive your work independently, but enjoy working in project teams from start to finish to achieve the goal. You are comfortable communicating on the phone/Teams and e-mail.

As a person, we further believe that you are outgoing and enthusiastic, a natural communicator, and can adapt your approach depending on the situation. You work as a team player and apply communicative and interactive skills on different levels within the organization and with external parties and customers.

More information

For more information about the position, please contact Sofia Löwstedt, HR Director, at [email protected] or +46707158790.

Please submit your application via this link with a short personal letter and your CV included, no later than June 6, 2021.

The position is ideally based in our Uppsala or Mölndal office in Sweden but could possibly be placed internationally home-based in the US or Europe.

About Antaros Medical

At Antaros Medical, we combine ground-breaking imaging with profound experience in drug development and deep knowledge of disease mechanisms. We are specialised in cardiorenal & metabolic diseases and oncology. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI) and COST. Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden. Visa mindre

Are you interested in image analysis in clinical trials? Would you like to work in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? If this catches your interest, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development.

To deliver on our commitments, we are looking for people with both broad and deep experience in clinical drug development as well as project management.

As a Study & Business Coordinator, you will be responsible for coordination in and administration of our clinical trials. The role may also include overall administrative support in driving our business forward. The position will be located in our office in Uppsala or Mölndal.

Main responsibilities:

- Provide general administrative support and assistance to the internal project team, primarily the Project Manager.
- Support the internal project team with ongoing conduct of studies including coordination of administrative tasks during the study process
- Contribute to applications & submissions by handling clinical-regulatory documents
- Assist in contact with clinical sites for specific requests (e.g., enrollment updates, missing documentation, meeting arrangements).
- Attend project team meetings and generate meeting minutes.
- Set up, organize, and maintain clinical study documentation in the trial master file
- Quality control of and archival of the TMF after final study
- Collaboration with third-party archive vendor
- General company administration, such as travel booking, expenses, presentations, meetings, etc


Requirements:

- Experience from working with clinical trials and according to ICH-GCP
- Level of education that supports skills and capabilities of the position and ensures successful conduct of responsibilities
- Collaboration skills in order to engage with people and clients
- Proven administrative skills
- Excellent knowledge of spoken and written Swedish and English


More information

For more information about the position, please contact Sofia Löwstedt, HR Director, +46 707 15 87 90



Please submit your application via this link with a short personal letter and your CV included, no later than May 2, 2021. We only accept applications via our recruitment system, Teamtailor. The recruitment is handled by Antaros Medical.

About Antaros Medical

At Antaros Medical, we are specialised in cardiometabolic diseases (including NAFLD/NASH and chronic kidney disease) and oncology. We have established ourselves as a strategic development partner to the pharmaceutical industry, where we combine ground-breaking imaging with profound experience in drug development and deep knowledge in disease mechanisms. Our projects cover clinical trials in all stages of drug development, and we work both with small biotech companies as well as global big pharma companies. We currently have around 90 employees working at our offices in Mölndal and Uppsala. Visa mindre

Would you like to work as an MR Imaging Specialist in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? If this ticks your boxes, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development. We currently have around 90 employees working at our offices in Sweden (Mölndal and Uppsala) and we are continuously growing and developing. As a part of our growth journey, we are now looking for an MR Imaging Specialist. The role will be based in either Uppsala or Mölndal.

As an MR Imaging Specialist, you will be involved in the start-up and operational phase of clinical trials ensuring the best quality of MR images collected on the clinical imaging sites participating in our contract research studies and as part of our own R&D. Your main focus will be responsibility for setting up harmonized imaging protocols, training the sites on the procedures and communicating with imaging site staff.

You will join a group of imaging specialists with expertise in MR and PET, and you will be working closely with Imaging Scientists, Project Managers, and Image Analysts to deliver innovative imaging solutions to the pharmaceutical industry.

An important aspect of your job will be assuring image quality in clinical studies, including on-site and remote training and assessment of clinical imaging sites. You will be helping the imaging sites with the setting up of imaging protocols according to study requirements and educating them on the processes to be followed in the clinical trials that we work on.

Your main responsibilities will be:

- Managing imaging aspects of clinical trials
- Training and qualifying imaging sites


Requirements:

- A radiographer’s degree, specialization in MRI
- Extensive clinical MRI experience working as a radiographer or similar
- Experience in working with MRI scanners from multiple vendors
- Strong communication skills in English (written and oral)


Preferred qualifications:

- Experience in abdominal imaging
- Experience in working according to GCP and in clinical trials
- Experience in the pharmaceutical or medical technology industries


Who are we looking for?

We believe that you have strong organizational skills and drive your work independently, but enjoy working in project teams from start to finish to achieve the goal. You are comfortable communicating on the phone/Teams and e-mail.

As a person, we further believe that you are outgoing and enthusiastic, a natural communicator, and can adapt your approach depending on the situation. You work as a team player and apply communicative and interactive skills on different levels within the organization and with external parties and customers.

More information

For more information about the position, please contact Sofia Löwstedt, HR Director, at [email protected] or +46707158790.

Please submit your application via this link with a short personal letter and your CV included, no later than June 6, 2021. Visa mindre

Are you interested in image analysis in clinical trials? Would you like to work in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? If this catches your interest, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development.

To deliver on our commitments, we are looking for people with both broad and deep experience in clinical drug development as well as project management.

As a Clinical Trial Assistant, you will be responsible for coordination in and administration of our clinical trials. The role may also include overall administrative support in driving our business forward. The position will be located in our office in Uppsala or Mölndal.

Main responsibilities:

- Provide general administrative support and assistance to the internal project team, primarily the Project Manager.
- Support the internal project team with ongoing conduct of studies including coordination of administrative tasks during the study process
- Contribute to applications & submissions by handling clinical-regulatory documents
- Assist in contact with clinical sites for specific requests (e.g., enrollment updates, missing documentation, meeting arrangements).
- Attend project team meetings and generate meeting minutes.
- Set up, organize, and maintain clinical study documentation in the trial master file
- Quality control of and archival of the TMF after final study
- Collaboration with third-party archive vendor
- General company administration, such as travel booking, expenses, presentations, meetings, etc


Requirements:

- Experience from working with clinical trials and according to ICH-GCP
- Level of education that supports skills and capabilities of the position and ensures successful conduct of responsibilities
- Collaboration skills in order to engage with people and clients
- Proven administrative skills
- Excellent knowledge of spoken and written Swedish and English


More information

For more information about the position, please contact Sofia Löwstedt, HR Director, +46 707 15 87 90



Please submit your application via this link with a short personal letter and your CV included, no later than May 2, 2021. We only accept applications via our recruitment system, Teamtailor. The recruitment is handled by Antaros Medical.

About Antaros Medical

At Antaros Medical, we are specialised in cardiometabolic diseases (including NAFLD/NASH and chronic kidney disease) and oncology. We have established ourselves as a strategic development partner to the pharmaceutical industry, where we combine ground-breaking imaging with profound experience in drug development and deep knowledge in disease mechanisms. Our projects cover clinical trials in all stages of drug development, and we work both with small biotech companies as well as global big pharma companies. We currently have around 90 employees working at our offices in Mölndal and Uppsala. Visa mindre

Are you interested in image analysis in clinical trials? Would you like to work in a growing company that is devoted to making a real difference within drug development through ground-breaking imaging? A place that constantly is moving forward, with great science, great people, and an informal atmosphere? If this sounds interesting, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical trials for decision making and differentiation in drug development. We are specialised in cardiometabolic diseases (including NAFLD/NASH and chronic kidney disease) and oncology. We have established ourselves as a strategic development partner to the pharmaceutical industry, where we combine ground-breaking imaging with profound experience in drug development and deep knowledge in disease mechanisms. Our projects cover clinical trials in all stages of drug development, and we work both with small biotech companies as well as global big pharma companies. We experience steady growth and currently have around 80 employees working at our offices in Mölndal and Uppsala, and we recently opened a subsidiary in US.

To deliver on our commitments, we are now looking for people with experience in clinical drug development t.

As Clinical Project Manager at Antaros Medical, you will be overall responsible and accountable for the execution of assigned projects from initiation to end of the project ensuring that the projects are delivered to budget, high quality, and timelines. The position can be located in our office in Mölndal or Uppsala.

As Clinical Project Manager at Antaros Medical, your main responsibilities will be:

- Project management of the imaging part in clinical trials to ensure our trials are delivered on time, to the agreed budget, and to high quality, per internal and client’s SOPs, ICH/GCP, and other regulation
- In parallel manage multiple projects ranging in size and complexity from single to multicenter studies
- Act as a primary contact to the client to ensure smooth operations and communication
- Manage the internal trial team to ensure the right input at the right time from different skills within the company
- Present project information at internal and external meetings
- Responsible for risk management and lessons learned for assigned projects
- Manage the project financials in collaboration with the Finance Department and financial follow-up for assigned projects


Requirements:

- University degree in life sciences
- At least 3 years experience from working with clinical trials from start to end
- Experience within project management of clinical trials is preferred
- Strong understanding of ICH-GCP and other relevant regulations and guidelines in relation to clinical trials
- Understanding of the full drug development process
- Excellent written and verbal communication skills in both Swedish and English
- Flexibility and ability to handle multiple tasks and projects to meet deadlines while delivering high-quality work in a dynamic environment
- Demonstrated collaboration skills as well as a team-oriented approach to engage with colleagues and clients


More information

For more information about the position, please contact Caroline Engvall, Chief Operating Officer, +46 733 319 112.

Please submit your application via this link with a short personal letter and your CV included, no later than April 18 2021. Interviews will be performed throughout the application period. We only accept applications via our recruitment system, Teamtailor. The recruitment is handled by Antaros Medical. Visa mindre

Are you interested in image analysis in clinical trials? Would you like to work in a growing company that is devoted to making a real difference within drug development through ground-breaking imaging? A place that constantly is moving forward, with great science, great people, and an informal atmosphere? If this sounds interesting, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical trials for decision making and differentiation in drug development. We are specialised in cardiometabolic diseases (including NAFLD/NASH and chronic kidney disease) and oncology. We have established ourselves as a strategic development partner to the pharmaceutical industry, where we combine ground-breaking imaging with profound experience in drug development and deep knowledge in disease mechanisms. Our projects cover clinical trials in all stages of drug development, and we work both with small biotech companies as well as global big pharma companies. We experience steady growth and currently have around 80 employees working at our offices in Mölndal and Uppsala, and we recently opened a subsidiary in US.

To deliver on our commitments, we are now looking for people with experience in clinical drug development t.

As Clinical Project Manager at Antaros Medical, you will be overall responsible and accountable for the execution of assigned projects from initiation to end of the project ensuring that the projects are delivered to budget, high quality, and timelines. The position can be located in our office in Mölndal or Uppsala.

As Clinical Project Manager at Antaros Medical, your main responsibilities will be:

- Project management of the imaging part in clinical trials to ensure our trials are delivered on time, to the agreed budget, and to high quality, per internal and client’s SOPs, ICH/GCP, and other regulation
- In parallel manage multiple projects ranging in size and complexity from single to multicenter studies
- Act as a primary contact to the client to ensure smooth operations and communication
- Manage the internal trial team to ensure the right input at the right time from different skills within the company
- Present project information at internal and external meetings
- Responsible for risk management and lessons learned for assigned projects
- Manage the project financials in collaboration with the Finance Department and financial follow-up for assigned projects


Requirements:

- University degree in life sciences
- At least 3 years experience from working with clinical trials from start to end
- Experience within project management of clinical trials is preferred
- Strong understanding of ICH-GCP and other relevant regulations and guidelines in relation to clinical trials
- Understanding of the full drug development process
- Excellent written and verbal communication skills in both Swedish and English
- Flexibility and ability to handle multiple tasks and projects to meet deadlines while delivering high-quality work in a dynamic environment
- Demonstrated collaboration skills as well as a team-oriented approach to engage with colleagues and clients


More information

For more information about the position, please contact Sofia Löwstedt, HR Director, +46 707 15 87 90

Please submit your application via this link with a short personal letter and your CV included, no later than April 18, 2021. Interviews will be performed throughout the application period. We only accept applications via our recruitment system, Teamtailor. The recruitment is handled by Antaros Medical. Visa mindre

Are you interested in an innovative company characterized by an entrepreneurial and inspiring spirit? A company, where you would be valued for your competence, ideas and creativity? A place, where relations and trust are keys to success and where we all value having fun while doing a meaningful job? If this sounds interesting, we may have the perfect offer for you.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development. We are specialized in cardiorenal and metabolic diseases (including NAFLD/NASH and chronic kidney disease) and oncology. We have a global network of partners and customers, including both large and small drug development companies, and we are a partner in several European research consortia, such as the Innovative Medicine Initiative (IMI) and COST. We are based in the BioVentureHub in Mölndal and in Uppsala Science Park, Sweden and recently, we opened a subsidiary in US.

Since we are growing, we are now looking for a Director MR Imaging - an exciting and diverse role at Antaros Medical. As a Director MR Imaging, you will be involved in the design of clinical trials ensuring the best MR methods are applied in our contract research studies and as part of our own R&D. Your main focus will be responsibility for setting up harmonized imaging protocols, selecting and qualifying the participating imaging sites, and training the Antaros Corelab on analysis methods.

You will join a group of imaging specialists with expertise in MR and PET, and you will be working closely with project managers, image analysts and software developers to deliver innovative imaging solutions to the pharmaceutical industry.

An important aspect of your job will be visiting imaging sites to set-up imaging protocols, which means you should be able to travel regularly, have good social skills and fluency in English. Preferably, you also have experience of working hands-on at the scanner. The job encourages interaction with new potential customers as part of the Antaros Medical sales strategy. Method development is a core activity at Antaros Medical, and scientific communication is an important channel to share our results. We therefore encourage scientific publishing and presenting on international scientific congresses.

You will have a scientific background in MR imaging. You drive your work independently but enjoy working in project teams from start to finish to achieve the goal. Experience in the pharmaceutical or medical technology industries is an advantage.

Your main responsibilities will be:

- Managing imaging aspects of clinical trials
- Developing analysis methods, training and certifying Corelab image analysts


Additional responsibilities could include:

- Communication with new customers, supporting sales and business development
- Scientific communication (writing publications and presenting research)


Requirements:

- A Ph.D. degree in a relevant field or comparable work experience
- Experience in Magnetic Resonance Imaging.
- Flexibility and ability to handle multiple tasks to meet deadlines while delivering high quality work in a dynamic environment.
- Demonstrated collaboration skills as well as a team-oriented approach to engage with colleagues and clients.


Preferred qualifications:

- Experience in abdominal imaging
- Good understanding of the physiological/pathology behind imaging endpoints
- Experience in scientific communication (publishing and presenting)
- Experience in GCP and clinical trials
- Experience in spectroscopic imaging


The position is based at our Uppsala or Mölndal offices in Sweden, or our Richmond office in USA.

More information

For more information about the position, please contact Sofia Löwstedt, HR Director [email protected] or +46707158790.

Please submit your application via this link with a short personal letter and your CV included, no later than August 9, 2020. Visa mindre

Would you like to work in a growing biotech company that is devoted to make real difference within drug development through ground-breaking imaging and extensive expertise in disease biology? A place that constantly is moving forward, with great science, great people (from all over the world), and an informal atmosphere? A company where the HR aspects are highly prioritized and where we value having fun while doing a meaningful job? If this sounds interesting, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development. We are specialised in cardiometabolic diseases (including NAFLD/NASH and chronic kidney disease) and oncology. We have established ourselves as a strategic development partner to the pharmaceutical industry, where we combine ground-breaking imaging with profound experience in drug development and a deep knowledge in disease mechanisms. Our projects cover clinical trials in all stages of drug development, and we work both with small biotech companies as well as global big pharma companies. We have currently around 60 employees working at our offices in Mölndal and Uppsala, and recently we opened a subsidiary in US.

People and culture are an important aspect of our work. As an employer, we believe that good HR processes are essential for a thriving work environment, and so is recruiting and retaining our great people. To further strengthen this perspective, we are now looking for a skilled HR assistant that will support our Director, HR with our recruitment processes and the coordination of our HR processes.

Main responsibilities:

- Support our recruitment process
- Provide general administrative support and assistance to various HR processes
- Coordinate employee onboarding and offboarding
- Coordinate relocation and migration processes
- Manage HR documentation, policies and administration
- Manage our recruitment system
- Support our work environment processes
- Coordinate engagement activities


Skills and education

We believe that you are a driven, curious, and service minded person. To thrive in this role, it is important that you have strong administrative skills as well as an analytical and proactive mindset. You will be working in a broad HR setting, which requires a structured mindset as well as an understanding of the bigger picture. Further, we believe that you have strong communication skills, and enjoy producing results by collaborating with others.

Requirements:

- An academic degree in HR or similar
- 1-2 years HR/and or Recruitment experience
- Excellent written and verbal communication skills in both Swedish and English


More information

For more information about the position, please contact Sofia Löwstedt, Director HR +46 707 15 87 90 or [email protected]. During the summer, we will not be able to answer between July 9th and August 10th.

Please submit your application via this link with a short personal letter and your CV included, no later than August 9th, 2020. We only accept applications via our recruitment system, Teamtailor. The recruitment is handled by Antaros Medical. Visa mindre

Would you like to work in a growing biotech company that is devoted to make real difference within drug development through ground-breaking imaging and extensive expertise in disease biology? A place that constantly is moving forward, with great science, great people (from all over the world), and an informal atmosphere? A company where the HR aspects are highly prioritized and where we value having fun while doing a meaningful job? If this sounds interesting, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development. We are specialised in cardiometabolic diseases (including NAFLD/NASH and chronic kidney disease) and oncology. We have established ourselves as a strategic development partner to the pharmaceutical industry, where we combine ground-breaking imaging with profound experience in drug development and a deep knowledge in disease mechanisms. Our projects cover clinical trials in all stages of drug development, and we work both with small biotech companies as well as global big pharma companies. We have currently around 60 employees working at our offices in Mölndal and Uppsala, and recently we opened a subsidiary in US.

People and culture are an important aspect of our work. As an employer, we believe that good HR processes are essential for a thriving work environment, and so is recruiting and retaining our great people. To further strengthen this perspective, we are now looking for a skilled HR coordinator that will support our Director, HR with our recruitment processes and the coordination of our HR processes.

Main responsibilities:

- Support our recruitment process
- Provide general administrative support and assistance to various HR processes
- Coordinate employee onboarding and offboarding
- Coordinate relocation and migration processes
- Manage HR documentation, policies and administration
- Manage our recruitment system
- Support our work environment processes
- Coordinate engagement activities


Skills and education

We believe that you are a driven, curious, and service minded person. To thrive in this role, it is important that you have strong administrative skills as well as an analytical and proactive mindset. You will be working in a broad HR setting, which requires a structured mindset as well as an understanding of the bigger picture. Further, we believe that you have strong communication skills, and enjoy producing results by collaborating with others.

Requirements:

- An academic degree in HR or similar
- 1-2 years HR/and or Recruitment experience
- Excellent written and verbal communication skills in both Swedish and English


More information

For more information about the position, please contact Sofia Löwstedt, Director HR +46 707 15 87 90 or [email protected]. During the summer, we will not be able to answer between July 9th and August 10th.

Please submit your application via this link with a short personal letter and your CV included, no later than August 9th, 2020. We only accept applications via our recruitment system, Teamtailor. The recruitment is handled by Antaros Medical. Visa mindre