Principal Medical Writer
BeOne Medicines
full-time
Posted on:
Location Type: Remote
Location: Massachusetts • United States
Visit company websiteExplore more
Salary
💰 $137,100 - $171,400 per year
Job Level
About the role
- Provide expertise to support the development of clinical and regulatory documents
- Mentor junior MWs as needed
- Manage multiple documents including complex ones
- Collaborate with study teams for document development
- Create and maintain document writing templates and guidance
- Identify potential risks and make mitigation plans
- Provide technical mentorship to junior MWs
- Share regulatory writing knowledge across teams
Requirements
- PhD in Biotechnology, Engineering, Biochemistry, or a related quantitative discipline with 2 years experience, OR Master’s degree with 5 years experience
- Writing clinical study reports
- Writing protocols
- Writing protocol amendments
- Analyzing, Synthesizing, and Presenting Complex Information
- Working with regulatory authorities from multiple regions
Benefits
- Medical
- Dental
- Vision
- 401(k)
- FSA/HSA
- Life Insurance
- Paid Time Off
- Wellness
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical study reportsprotocolsprotocol amendmentsanalyzing informationsynthesizing informationpresenting information
Soft Skills
mentoringcollaborationrisk identificationtechnical mentorship
Certifications
PhD in BiotechnologyPhD in EngineeringPhD in BiochemistryMaster’s degree in related discipline