Medical Affairs Director/Senior Manager
Salary/Rate:70,000EUR - 90,000EUR
Job type:Perm
Town/City:Remote
Country:Germany
Business Sectors:Regulatory Affairs, Clinical
Job ref:25042
Post Date:22. 03. 2024
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About the Role
Medical Affairs Director/Senior Manager
Are you an expert in Medical/Clinical Affairs in Class III Implantable Devices?
Are you looking to take your next step into a leadership role?
Do you want to work with a global technology leader in regenerative medicine?
We are currently supporting our client headquartered in Germany to strengthen their clinical/medical affairs function. This is a remote role, so you can be based anywhere in Germany but must be willing to travel from time to time.
Does this sound like your next career step?
Tasks
Please apply with your CV or contact May-Lynn Capocciama-Knecht for further details on this opportunity and additional vacancies in R&D, Regulatory Affairs and Quality Management.
may-lynn.ck@adaptivelifescience.com
+49 30 1663 7750
#LI-MC2
Are you an expert in Medical/Clinical Affairs in Class III Implantable Devices?
Are you looking to take your next step into a leadership role?
Do you want to work with a global technology leader in regenerative medicine?
We are currently supporting our client headquartered in Germany to strengthen their clinical/medical affairs function. This is a remote role, so you can be based anywhere in Germany but must be willing to travel from time to time.
Does this sound like your next career step?
Tasks
- Management of a small team (2-5 employees)
- Ensure regulatory compliance for clinical trials and medical products on the market in accordance to MDR, TGA and FDA
- Pre-market and post-market clinical projects, including medical writing, CERs, PMS, and PMCFs
- Clinical trial project management (documentation, budget planning, collaboration with stakeholders on an international level as well as CROs)
- Reimbursement and compliance (Europe, especially Germany)
- Degree in a scientific field such as biomedical, biology, medicine, medical engineering or a comparable field of study
- Experience in clinical (e.g. CER), regulatory affairs, bio-medical publication or medical writing, especially for class III implants
- Strong communication skills and project management experience
- Team player who can also work independently
- Knowledgeable in MS Office
- Fluency in English, German is a bonus
Please apply with your CV or contact May-Lynn Capocciama-Knecht for further details on this opportunity and additional vacancies in R&D, Regulatory Affairs and Quality Management.
may-lynn.ck@adaptivelifescience.com
+49 30 1663 7750
#LI-MC2