Senior Medical Writer — Regulatory & Clinical Documentation Lead
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Science
Medical Science Liaison, Healthcare Compliance
Job Description & How to Apply Below
Bio Marin is seeking a Senior Medical Writer to author and edit regulatory documents and clinical study materials. You will work with cross-functional teams to ensure high-quality, compliant submissions across INDs, BLA/NDAs, and safety reports.
Responsibilities include coordinating study team reviews, developing timelines, and guiding document templates. A scientific background and strong communication skills are essential to align with regulatory expectations and project goals.
We invite applications for the Senior Medical Writer — Regulatory & Clinical Documentation Lead position located in Home, KS, United States.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Senior Medical Writer — Regulatory & Clinical Documentation Lead role in the description above.
We appreciate your interest in this position.
Position Requirements
10+ Years work experience(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).