Associate Director Medical Writing (Hybrid)

General Summary:
The Associate Director, Medical Writing Science manages overall operations of a team or major project through effective leadership. Provides guidance and leadership for document development for regulatory filings and coordinates clinical sections of complex regulatory submissions (organization, content, and resourcing). Applies advanced technical expertise to solve complex problems, foster interdisciplinary understanding, and integrate Medical Writing Science activities with other departments.

Key Duties and Responsibilities:
- Independently author routine and complex clinical and regulatory documents
- Provide strategic input into program-level plans
- Align, coordinate, and build consistent information and messages across clinical program(s)
- Provide leadership for Medical Writing Science and manage a team
- Develop and implement goals and initiatives for Medical Writing Science
- Facilitate implementation of new technologies and initiatives for clinical document preparation
- Anticipate risks, solve complex problems, and implement process improvements

Knowledge and Skills:
- Plan, manage, and optimize department resources (e.g., staff, technology)
- Lead independently; solve non-routine, complex problems across broad issues
- Anticipate problems and prepare contingency plans
- Understand scientific disciplines beyond own specialty
- Manage direct reports and guide staff development
- Experience with marketing authorization application regulatory submissions

Education and Experience:
- Bachelor’s degree in a relevant discipline
- Ph.D. (or equivalent)
- Typically requires 8 years of work experience and 2 years of supervisory/management experience (or equivalent)

Hybrid work: 2 days/week remote and 3 days/week in Boston Fan Pier office.

Pay Range: $157,600–$236,400. Eligible for annual bonus and annual equity awards.