Medical Writing Manager (Hybrid)
Vertex Pharmaceuticals · Boston, MA
Medical AffairsFull-time$120k–$180kCompany career page
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Role summary
Vertex Pharmaceuticals seeks a Medical Writing Science Manager to author clinical regulatory documents and lead moderately complex clinical studies. The role requires scientific expertise in drug development and cross-functional collaboration to support product development initiatives.
What they're looking for
- Ph.D. or equivalent degree
- 4 years medical writing or related experience
- Proficiency writing clinical regulatory documents
- Knowledge of drug development, clinical research, biostatistics, and regulatory requirements
- Superior written and oral communication skills
- Advanced proficiency with word processing, templates, and document management systems
- Strong project management and team coordination abilities
What you'll be doing
- Author moderately complex clinical regulatory documents including protocols, study reports, and investigator's brochures
- Lead medical writing activities for moderately complex clinical studies
- Analyze and interpret clinical study data to support document composition and regulatory submissions
- Develop key messages and ensure scientific consistency across related documents and programs
- Contribute scientific input to product development plans and serve as coordinating author
Privacy & handoff
This role links to Vertex Pharmaceuticals'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.