Associate Director, Medical Writing (Hybrid - SF Bay Area)

We are seeking an experienced Associate Director of Medical Writing to lead the development of high-quality clinical and regulatory documents in support of complex drug development programs. This individual will play a key role in shaping document strategy, ensuring scientific accuracy, and driving cross-functional alignment across clinical, regulatory, and biostatistics teams.

This is a hybrid role based in the San Francisco Bay Area . Relocation package is available.

Key Responsibilities

• Lead the planning, authoring, and review of clinical and regulatory documents, including clinical study reports (CSRs), protocols, investigator brochures (IBs), and submission documents
• Serve as the medical writing lead on complex, multi-phase programs, including late-stage development and regulatory submissions ...