Tasks

- Developing, revising and reviewing the clinical evaluation plans and reports, as well as other documents submitted to the regulatory authorities
- Providing support in the risk assessment process
- Interacting with other departments

Qualifications

- MD or PhD in a Life Science subject, preferably in Cardiovascular Science
- First exposure to the medical device industry, at least 2 years of experience in medical writing
- Fluent in English

Additional Information

Part-time position, mostly remote.