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IC Medical Writer- 6 month contract

Hydrogen Group

Job Description

Collaborating with the clinical & regulatory teams to write clinical documents for regulatory submissions.

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*Hours will fluctuate

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  • 10 years Regulatory Writing experience for pharmaceutical industry.
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  • Lead author experience required
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  • Experience with NDA modules and higher level module writing as well as CSRs, IBs, protocols, etc.
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  • Phase II/III experience
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  • Neuroscience or CNS related drug indication experience
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  • Advanced degree (Ph.D, MD, Sc.D, MA/MS or MPH).
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Vacancy posted 10 days ago
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