Job Details

We are seeking an experienced medical writing leader to oversee the development of high-quality clinical and regulatory documents. This role will provide strategic guidance across programs and manage a team of writers and external partners. This is a hybrid role based in Redwood City, offering the opportunity to contribute to a dynamic and growing clinical development team.

Job Title

Director, Medical Writing

Responsibilities

• Oversee the development of high-quality clinical and regulatory documents.
• Provide strategic guidance across programs.
• Manage a team of writers and external partners.

Key Qualifications

• Proven line management experience, including mentoring and leading direct reports.
• Strong background in regulatory medical writing across clinical development programs.
• Excellent communication, project management, and cross-functional collaboration skills.
• Familiarity with global regulatory requirements and document standards.
• Proficiency with document management systems and writing tools.

Education

Bachelor's degree in a scientific discipline required; advanced degree (PhD, PharmD, MS) preferred.

Seniority level

• Director

Employment type

• Full-time

Job function

• Management and Writing/Editing

Industries

• Biotechnology Research and Pharmaceutical Manufacturing

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