Clinical Documentation Jobs
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Summary: The Chemistry Manufacturing and Controls (CMC) Technical Writing function resides organizationally within Regulatory Affairs. The CMC Techni
This is an exciting opportunity to work within a fast paced environment at AnaptysBio, which...
As a member of the Bulletproof family, you'll enjoy a culture that values diversity in all things - people, work, experience levels, and much more. We
TP Therapeutics is seeking a Director/Senior Director, Clinical Pharmacology, to provide clinical pharmacology strategy on our drug development.
The Senior Manager is responsible for leading the team members, activities and initiatives for the AbbVie Archive. This department archives records fr
Scientific Writer SUMMARY: Provide technical expertise in creating and managing strategic scientific content. RESPONSIBILITIES: Spearhead the ...
Bristol-Myers Squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients p
Position OverviewServes as a point of contact for processes, systems and controls for Standard Operating Procedures (SOPs), Trial Master Files (TMF),
Associate Technical Writer:The Associate Technical Writer, is responsible for preparing CMC elements of regulatory filings under a Technical Writer's
The Scientist/Technical Writer, is responsible for managing and preparing the entire drug substance and drug product analytical sections of regulatory
Bring your desire to learn, attention to detail, adaptability, and your ability to contribute to a high performing team to Corvus!
Responsibilities Lead, manage and co-ordinate the conduct of assigned clinical trials from study start-up to close out in accordance with ICH-GCP ...
The Senior Medical Writing Scientist is responsible for preparing moderately complex clinical study documents and sections of regulatory submissions.