IC Medical Writer- 6 month contract

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).