IC Medical Writer- 6 month contract
Hydrogen Group
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).
Vacancy posted 9 hours ago
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