IC Medical Writer- 6 month contract
hydrogen groupLos Angeles (CA)
About the role
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).
Before you apply
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Your profile is current
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Two examples you can talk through
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A number in mind
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Your notice period
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Once you apply, someone reads it and calls you before anything reaches the employer — usually within two working days.
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