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Medical WritingPharmaceuticalsSenior
Senior Medical Writer, Regulatory
Remote (US)Permanent$115,000 – $145,000Posted 2 weeks ago
About the role
Write and coordinate clinical and regulatory documents for late-stage programs across therapeutic areas.
What you’ll do
- Author clinical study reports, protocols, and CTD summaries.
- Lead document review cycles with cross-functional authors.
- Ensure consistency, quality, and compliance with templates.
- Manage timelines across concurrent deliverables.
What you’ll bring
- 6+ years of regulatory medical writing experience.
- Command of ICH E3 and CTD authoring conventions.
- Excellent scientific writing and project management.
- Advanced degree in life sciences preferred.
Bektin is an equal-opportunity partner. We present every qualified candidate on merit and keep your details confidential until you approve a submission.