
Medical Writing Manager – FSP
Thermo Fisher Scientific
full-time
Posted on:
Location Type: Remote
Location: North Carolina • United States
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About the role
- Manage, mentor, and develop Medical Writers to ensure exceptional performance and continuous growth
- Supervise and review the preparation of a wide range of medical writing deliverables
- Ensure projects are completed on time and to the highest scientific and regulatory standards
- Deliver compelling capabilities presentations to prospective clients
- Contribute to the development, evaluation, and improvement of SOPs and work practices
Requirements
- Bachelor’s degree in a life science field (advanced degree—PharmD, PhD, MSc—preferred)
- 5+ years of relevant regulatory writing experience, including at least 2 years in medical writing within pharma/CRO and 1+ year of leadership responsibility
- Exceptional writing, editorial, and data interpretation skills
- Strong project management ability—forecasting, timelines, resource allocation
- Excellent communication and presentation skills, especially in client-facing settings
- Ability to manage complexity, multitask, and work in a fast-paced environment
Benefits
- award-winning learning and development programme
- competitive salary
- extensive benefits package
- flexible working culture
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
regulatory writingmedical writingdata interpretationproject managementSOP developmentediting
Soft skills
mentoringcommunicationpresentationleadershipmultitaskingtime management
Certifications
Bachelor’s degreePharmDPhDMSc