Senior Medical Writer — Regulatory Strategy & Mentorship

A global biotechnology company seeks a Principal Medical Writer to support the development of high-quality clinical and regulatory documents in Cambridge, MA. The ideal candidate will have a PhD or Master’s in a relevant field, with significant experience in writing clinical documents. Responsibilities include mentoring junior writers and managing complex documentation tasks. This role allows for full-time telecommuting, offering a competitive salary and a comprehensive benefits package. #J-18808-Ljbffr