At a Glance
- Tasks: Draft and edit regulatory documents for clinical studies and safety reports.
- Company: Join BioMarin, a leader in innovative biopharmaceuticals.
- Benefits: Enjoy a hybrid work model, competitive salary, and career development opportunities.
- Other info: Collaborate with cross-functional teams in a dynamic and supportive environment.
- Why this job: Make a difference in healthcare by contributing to vital clinical research.
- Qualifications: Extensive medical writing experience and strong regulatory knowledge required.
The predicted salary is between 55000 - 65000 £ per year.
Bio Marin is seeking a Senior Medical Writer to join the Global Medical Writing function in a hybrid role with two days per week in the London office.
The candidate will draft and edit regulatory documents for clinical studies, work on safety reports, and prepare regulatory filings while collaborating with cross-functional teams across development science.
The role requires extensive medical writing experience, strong regulatory knowledge, and the ability to manage timelines and document reviews.
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