A company is looking for a Director, Medical Writing.
Key Responsibilities:
Lead the development of protocols and amendments within the Oncology therapeutic area
Optimize medical writing processes and templates for protocols
Oversee recruitment and manage medical writers and contractors
Required Qualifications:
PharmD/PhD with 8+ years’ relevant experience, MA/MS/MPH/MBA with 10+ years’ relevant experience, or BA/BS with 12+ years’ relevant experience
Working knowledge of global regulatory affairs
Leadership skills and presentation skills
Proven track record of managing large scale, complex projects
Relevant experience in clinical research and development or regulatory affairs
