Biogen Idec is hiring: Senior Medical Writer in Cambridge
Biogen Idec - Cambridge, MA, United States, 02140
Work at Biogen Idec
Overview
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Overview
About This Role
As our new Senior Medical Writer you will provide medical writing support for clinical and regulatory documents. You will interact with other medical writers, document quality reviewers, and cross-functional teams as you create, author, and manage documentation required for the conduct of clinical trials and regulatory submissions.
A successful candidate will participate in cross-functional teams, and may lead strategy discussions related to document development and influence decision making.
What You'll Do
- Independently prepare moderately complex clinical documents for one or more programs
- Coordinate preparation of clinical documents by other writers with minimal supervision
- Represent the Medical Writing department on cross-function teams
- Lead document-related meetings
- Review statistical analysis plans and clinical data reports, as needed
- Mentor junior writers on department processes related to document preparation
- Participate on departmental initiatives
Qualifications
Required Skills
- Master's required in a life science or health discipline
- 1+ years regulatory writing experience within a life science organization
- Ability to interpret data
- Solid understanding of standard clinical document types
- Solid understanding of internal and external guidelines related to document preparation
- Strong written and oral communication skills
- Strong organizational and meeting skills
Preferred Skills
- PhD