Medical Writing Manager (Hybrid)
Boston, Massachusetts, United StatesHybridFull Time$120,200–$180,400 yearMid LevelDoctorate Or Professional DegreeUnknown
Job Summary
The Medical Writing Manager is responsible for preparing moderately complex clinical and regulatory documents, serving as the lead Medical Writing Scientist for clinical studies, and supporting the Medical Lead in analyzing clinical study data. Key skills include superior written and oral communication, data analysis, a broad understanding of drug development and regulatory requirements, and the ability to manage project teams. Candidates must possess a Ph.D. and 4 years of relevant experience.
Required Qualifications
- Ph.D. (or equivalent degree)
- Typically requires 4 years of experience or the equivalent combination of education and experience
Desired Qualifications
- Experience writing and editing clinical regulatory documents
- Ability to manage project teams and form productive working relationships
- Excellent project management and organizational skills
- Advanced computer skills related to word processing and document management systems