Senior Clinical Affairs Specialist
Salary/Rate:65,000EUR - 80,000EUR depeding on experience
Job type:Perm
Town/City:Munich
Country:Germany
Business Sectors:Regulatory Affairs, Clinical
Job ref:25041
Post Date:22. 03. 2024
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About the Role
Senior Clinical Affairs Specialist
Are you interested in joining an award-winning company who are innovating in the field of cardiotherapy?
Are you experienced with pre-market and post-market clinical studies for active medical devices up to class III?
We're currently supporting a client in the medical device industry who are head-quartered just outside of Munich and are looking to strengthen their Clinical Affairs function.
This is a hybrid position, so you must be accessible to the site.
Could you be their new Senior Clinical Affairs Specialist?
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 interested in joining an award-winning company who are innovating in the field of cardiotherapy?
Are you experienced with pre-market and post-market clinical studies for active medical devices up to class III?
We're currently supporting a client in the medical device industry who are head-quartered just outside of Munich and are looking to strengthen their Clinical Affairs function.
This is a hybrid position, so you must be accessible to the site.
Could you be their new Senior Clinical Affairs Specialist?
Tasks
- Responsible for the strategy and execution of clinical evaluation for medical devices up to Class III
- Look after the conception and the evaluation of follow-up studies
- Collaborate with clinical partners for various research projects
- Provide scientific input while supporting other areas of the organization
- Provide mentorship and sharing your expertise with colleagues
- Degree in a technical or scientific field, ideally in the direction of medical technology
- Several years of experience in clinical evaluation and follow-up of active medical devices up to class III
- Solid foundational knowledge of relevant regulatory and normative requirements (MDR, ISO 14155, MDCG Guidance etc.)
- Team player who can also work independently
- Eager to learn attitude and willingness to share your knowledge
- Fluency in German and English
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