United States$195K - $230K per year10+ yrs expHealthcare
The Associate Director will own the medical writing strategy and author high-stakes clinical and regulatory documents, including protocols and NDA modules. They will also oversee medical writing vendors and build internal processes to ensure regulatory compliance and document quality.
United States$215K - $245K per year10+ yrs expOthers
The Director of Trial Master File will establish and maintain standards, processes, and oversight frameworks to ensure TMFs are complete, accurate, and inspection-ready. This role involves leading TMF activities across the clinical portfolio, managing vendor performance, and driving continuous quality improvements.
