Turn science into submission‑ready success‑led medical writing in a fast‑paced biotech setting.

Proclinical is seeking a Senior Manager, Medical Writing to join a dynamic team in the rare disease and biotechnology space. In this role, you will collaborate with cross‑functional project teams to develop high‑quality clinical documents while ensuring compliance with applicable regulations and standards. This hybrid position requires two days per week in the office.

Responsibilities

• Produce high-quality, timely writing deliverables, including clinical protocols, investigator brochures, clinical study reports, and related documents.
• Independently plan, write, edit, and format key clinical documents.
• Manage and facilitate the review and finalization process for documents created internally or by external consultants, contractors, and vendors.
• Represent Medical Writing on early‑phase or specific late‑phase project teams, coll...