Job Description

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 #J-18808-Ljbffr RBW Consulting

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