Senior Regulatory Medical Writer
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Job Description
Senior Regulatory Medical Writer leading development of clinical regulatory documents for a global pharmaceutical company. Collaborating with teams across Canada, Europe, the Americas, and Asia-Pacific.
Responsibilities:
- Lead the development lifecycle of Phase II–IV clinical regulatory documents
- Own document development from planning through final delivery
- Coordinate cross‑functional contributors and reviewers
- Interpret clinical data and translate results into regulatory documents
Requirements:
- Bachelor’s degree in life science
- Advanced degree in life sciences (Master’s or PhD) preferred
- Minimum 4 years of regulatory medical writing experience
- At least 2 years as a medical writing project lead
- Strong expertise in CSRs and Protocols
Benefits:
- Training
- Mentorship
- Access to a global network of experts
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