Medical Writing Director
4 days ago
Gilead Sciences is a leading biopharmaceutical company with over 35 years of experience in developing innovative therapies to tackle some of the world's biggest health challenges.
We are seeking an Associate Director Medical Writer to join our dynamic team. In this role, you will be responsible for authoring high-quality regulatory documents, including clinical study reports, investigator's brochures, and CTD summaries/overviews.
Key Responsibilities:- Author a wide range of regulatory documents, including CSRs, investigator's brochures, and CTD summaries/overviews.
- Represent Medical Writing on cross-functional teams, providing guidance on regulatory submission document strategies.
- Lead or advise others on complex projects or problems with broad impact.
- Ensure own work complies with established practices, policies, and processes, and any regulatory or other requirements.
- Bachelor's or advanced degree in life sciences or related field.
- Significant medical writing experience in the biopharma industry.
- Experience leading a broad range of medical writing or related deliverables.
- Demonstrated subject matter expertise in regulatory documentation.
- In-depth knowledge of current global and regional trends in medical writing and regulatory.
- A competitive salary: $170,000 - $200,000 per year, based on experience.
- A comprehensive benefits package, including medical, dental, and vision coverage.
- Opportunities for professional growth and development.
Gilead Sciences is an equal opportunity employer and welcomes applications from diverse candidates.
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