Principal Medical Writer
Thermo Fisher Scientific
full-time
Posted on:
Location Type: Remote
Location: Remote • 🇫🇷 France
Visit company websiteJob Level
Lead
About the role
- Research, write, and edit clinical study reports and study protocols
- Serve as primary author on complex documents
- Provide senior level review and mentorship for document preparation
- Ensure compliance with quality processes for assigned documents
- Develop and review best practices for optimal results
- Identify and resolve out-of-scope activities
- Represent the department in meetings
Requirements
- Bachelor's degree in a scientific discipline or equivalent
- 8+ years of relevant experience in medical writing
- Experience managing complex medical writing projects
- Additional medical writing qualifications (AMWA; EMWA; RAC) advantageous
- Significant knowledge of document development guidelines
- In-depth knowledge in specialty areas like preclinical or regulatory submissions
- Excellent data interpretation and writing skills
Benefits
- Award-winning learning and development programme
- Competitive salary
- Extensive benefits package focused on health and well-being
- Flexible working culture with a work-life balance
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
clinical study reportsstudy protocolsmedical writingdocument development guidelinesdata interpretation
Soft skills
mentorshipcompliancebest practices developmentproblem-solvingcommunication
Certifications
AMWAEMWARAC