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Principal Medical Writer
BeOne MedicinesPrincipal Medical Writer providing expertise for clinical and regulatory document development at BeOne. Mentoring junior writers and collaborating across teams to optimize processes and training.
About the role
Key responsibilities & impact- Provides expertise to support the development of high-quality clinical and regulatory documents
- Manages assigned writing tasks ensuring adherence to regulatory guidelines
- Navigates uncertainties to develop and manage timelines of individual and multiple documents
- Identifies needs for process/tool optimization and proposes solutions
- Leads development of new training programs for junior MWs
Requirements
What you’ll need- An advanced degree (MS/PhD/PharmD/MD) in life science, pharmacy, medical, or health-related science is preferred
- Bachelor's with 5+, MS with a minimum of 4+ years of regulatory document writing (or equivalent) experience, or PhD/PharmD/MD with a minimum of 2+ years of regulatory document writing (or equivalent) experience
- Technical expertise in Microsoft Word, Adobe Acrobat, and electronic document management systems
- Proficiency in Microsoft Outlook, Excel, and PowerPoint
Benefits
Comp & perks- Medical
- Dental
- Vision
- 401(k)
- FSA/HSA
- Life Insurance
- Paid Time Off
- Wellness
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
regulatory document writingprocess optimizationtraining program development
Soft Skills
project managementproblem-solvingleadershipcommunication
Certifications
advanced degreeMSPhDPharmDMD