Senior Medical Writer
Thermo Fisher Scientific · Shanghai, China
Medical AffairsFull timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Senior medical writing role focused on creating regulatory documents and clinical study reports. Responsibilities include authoring submissions, mentoring junior writers, and advising on document strategy and regulatory compliance.
What they're looking for
- Bachelor's degree in scientific discipline; advanced degree preferred
- 8+ years regulatory medical writing experience required
- Pharmaceutical or CRO industry experience preferred
- Professional certifications in medical writing (AMWA, EMWA, RAC) advantageous
- Advanced knowledge of global and regional document development guidelines
- Expertise in data interpretation and scientific writing with strong editorial skills
- Excellent project management and mentoring capabilities
What you'll be doing
- Author clinical study reports, study protocols, and regulatory submission documents for internal and external clients
- Lead writing team, review documents, and provide training and guidance to junior medical writers
- Advise on document development strategy, regulatory requirements, and industry best practices
- Collaborate with clients to enable effective communication and operational excellence
- Serve as backup program manager as needed
Privacy & handoff
This role links to Thermo Fisher Scientific's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.