Principal Medical Writer
Veristat LLC
Independently planning and preparing regulatory documents and medical communications, the full-time Principal Medical Writer will support all phases of product development while working remotely and collaborating with cross-functional teams. Key responsibilities Organize, analyze, interpret, and present scientific and statistical information in compliance with ICH and regulatory guidelines Collaborate with internal and external document production teams to ensure high-quality deliverables Prepare a range of regulatory documents to support product development initiatives Required qualifications Bachelor's degree required; science-related field preferred Minimum of 7 years of medical writing experience in a contract research organization or pharmaceutical/biotechnology setting Advanced knowledge of ICH and related regulatory guidelines Proficiency in Microsoft Office Suite, including advanced skills in Microsoft Word Strong interpersonal and communication skills #J-18808-Ljbffr Veristat LLC
Vacancy posted 3 days ago
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