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Medical Writer
Background: Work as part of a winning team in a global role at a major CRO. Office-based. Primary Duties: To research, create, edit, and coordinate the production of clinical documents, study reports and protocols associated with submissions to regulatory authorities. You will demonstrate a clear understanding of the drug development process and have a broad knowledge of GCP guidelines as well as a working knowledge of EMEA & FDA guidelines and… See original job posting →
Salary: Excellent salary plus benefits package
Location: Middlesex
Berkshire
Windsor, Berkshire
Chalfont St. Giles, Buckinghamshire
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