RemoteOtterRemoteOtterExplore 34 Remote Regulatory Documents Jobs
T.P.A
Telix Pharmaceuticals (Americas)
The Medical Writer will lead the writing process for clinical and regulatory documents in a dynamic pharmaceutical company.
S.C
Sidwell Company
Harris Healthcare is looking for a motivated Business Analyst to drive user stories and system requirements in healthcare software.
ELLIGO HEALTH RESEARCH
The Project Management Specialist coordinates and supports clinical trials, ensuring regulatory compliance and effective communication across departments.
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U014 (FCRS = US014) Novartis Pharmaceuticals Corporation
Lead the strategic planning and management of clinical programs as a Senior Clinical Development Medical Director.
AbbVie
Join AbbVie as a Principal Strategic Medical Writer to lead and create high-quality clinical and regulatory documents.
Ultragenyx Pharmaceutical
The Associate Director, Medical Writing is responsible for creating and coordinating clinical and regulatory documents to support rare disease medicine.
AbbVie
The Senior Scientist II will lead CMC teams and author regulatory documents for biologics drug substances.
Amgen
The Clinical Trials Disclosure Associate prepares and manages clinical regulatory documents for public disclosure in a telecommute role.
AbbVie
The Principal Strategic Medical Writer leads the writing of clinical and regulatory documents, ensuring alignment with project goals and compliance with regulations.
A.P
Acadia Pharmaceuticals
The Director of Medical Writing will lead the preparation of clinical and regulatory documents to support product development.
AbbVie
The Senior Scientist will author regulatory documents and lead CMC teams for biologics development.
CSL Plasma
The Local Quality Manager for UK and Ireland ensures GxP compliance and oversees the quality of pharmaceutical product distribution.
ELLIGO HEALTH RESEARCH
The Project Management Specialist supports clinical trials by coordinating project tasks and regulatory documentation.
C.E
Criterion Edge
Join Criterion Edge as a remote Medical Writer to produce high-quality regulatory and scientific documents.
Nuvalent
The Manager, Medical Writing will lead medical writing projects and ensure high-quality documentation for clinical trials at Nuvalent.