Senior Manager, Medical Writing

Produce high quality and on-time writing deliverables. Independently plan, write, edit, and format key documents, including clinical protocols, investigator brochures, clinical study reports, integrated safety and efficacy summaries and related documents. Facilitate/manage efficient review and finalization process for documents produced internally and/or externally by consultants, contractors and vendors. Represent Medical Writing on multiple early phase project teams or on specific late phase project teams and collaborate with the Director of Medical Writing to ensure proper planning and resourcing for upcoming project writing deliverables. Collaborate effectively with Biometrics, Clinical Operations, Clinical Development, Regulatory Affairs, Pre-Clinical Development, Program Management, Research, Quality, and Corporate Communications, as well as with external stakeholders. Serve as subject matter expert for clinical documents and their production. Contribute to SOP and template development and maintenance Bachelor's degree in Life Science with relevant writing expertise or in English/Communications with relevant science expertise. Advanced degree and/or professional certification/credentials preferred. Experience as a medical writer in the sponsor and/or CRO setting. Experience with regulatory submissions (CTA/IND/NDA/BLA) and knowledge of eCTD formatting is a plus. In-depth knowledge of Good Clinical Practices, FDA regulations, ICH guidelines, and the drug development process. Successful track record of managing multiple projects in a fast-paced and deadline-driven environment. Impeccable attention to detail and ability to complete writing assignments in a timely manner. Experience overseeing the work of contract writers is a plus. Must be proficient with Microsoft Windows, Word, Excel, and PowerPoint. Ability to travel approximately 10% is required.