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Remote-Eligible Regulatory Affairs Manager (Europe)
Job summary
A global biopharmaceutical company in Cambridge is seeking a Regulatory Affairs Manager to ensure compliance with regulatory requirements for clinical trials and product approvals. You will be responsible for managing submissions and developing regulatory strategies in collaboration with the team. The ideal candidate should have a scientific degree, strong communication skills, and experience in regulatory environments. This role offers flexibility to work from home with some days in the office.
Benefits
Qualifications
- Demonstrated experience in a similar role.
- Experience working with policies, procedures and SOPs.
- Experience in the regional regulatory environment.
Responsibilities
- Ensure that Amgen acquires and maintains required licenses for clinical trials.
- Support regulatory submissions for products.
- Participate in developing regional regulatory strategies.
Skills
Education
* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.