Collaborating with the clinical & regulatory teams to write clinical documents for regulatory submissions.
*Hours will fluctuate
- 10 years Regulatory Writing experience for pharmaceutical industry.
- Lead author experience required
- Experience with NDA modules and higher level module writing as well as CSRs, IBs, protocols, etc.
- Phase II/III experience
- Neuroscience or CNS related drug indication experience
- Advanced degree (Ph.D, MD, Sc.D, MA/MS or MPH).
IC Medical Writer- 6 month contract in remote at Unknown Company
This position is listed as full time and onsite.