2 scientific writer jobs at 2 companies in Smithfield, NC
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Principal Medical Writer
Raleigh or United States or Canada
HybridFull Time
7+ YOE7+ years writing clinical/regulatory documents; advanced regulatory knowledge; bachelor’s degree in medical/scientific discipline; MS Word expertise; strong project management, communication, and attention to detail.
Microsoft Word
2mo
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Principal Medical Writer
Durham or London
OnsiteFull Time
5+ YOEBachelor's in life/health/scientific field, 5+ years medical or regulatory writing in pharma, 3+ years regulatory dossier and CTD experience, 3+ years independently authoring protocols and clinical study reports; strong writing, teamwork, and regulatory knowledge.
Common Technical Document (CTD), International Council for Harmonisation (ICH), Good Clinical Practice (GCP)