Director/Sr Director/Head of Medical Writing- Full Time- Direct Hire- Hybrid NY,
Hydrogen Group, New York, NY, United States
Draft, edit and submit high quality, medically accurate documents including protocols and clinical study reports. Reporting to the Head of Clinical Development.
10 years Regulatory Writing experience for pharmaceutical industry.
Experience with NDA modules, Safety Evaluation Reports, CSRs, IBs, protocols, etc.
Lead Author experience
Advanced degree (Ph.D, MD, Sc.D, MA/MS or MPH).
10 years Regulatory Writing experience for pharmaceutical industry.
Experience with NDA modules, Safety Evaluation Reports, CSRs, IBs, protocols, etc.
Lead Author experience
Advanced degree (Ph.D, MD, Sc.D, MA/MS or MPH).