RemoteOtterRemoteOtterExplore 24 Remote Regulatory Documents Jobs
AbbVie
The Senior Scientist will author regulatory documents and lead CMC teams for biologics development.
Vifor Pharma
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.
D.M.T
4D Molecular Therapeutics
Join 4DMT as an Associate Clinical Trial Manager to support clinical trial activities and ensure compliance with regulatory standards.
ClinChoice
Join ClinChoice as a Clinical Research Associate to monitor clinical trials and ensure compliance with regulatory standards.
Apogee Therapeutics
Seeking a Senior Manager for Medical Writing to provide clinical and regulatory document support in a dynamic biotech environment.
D.M
Disc Medicine
Disc Medicine is seeking a Director for Cell Line and Upstream Process Development to lead biologics program pipeline development.
Celerion
Celerion is seeking a full-time Senior Pharmacokinetic Scientist to conduct data analysis and report writing in a remote role based in the UK.
Nurix
Nurix
Nurix Therapeutics is seeking a Toxicology Scientist to lead and manage safety pharmacology and toxicology studies in drug development.
Indero
The Project Coordinator supports site activation activities and ensures quality deliverables throughout the clinical trial lifecycle.
Celerion
Join Celerion as a Senior Pharmacokinetic Scientist to conduct data analysis and report writing in a remote role.
T.P.A
Telix Pharmaceuticals (Americas)
Telix Pharmaceuticals is seeking a Medical Writer to lead the writing of clinical and regulatory documents for drug development.
Spyre Therapeutics
The Senior Medical Writer will develop high-quality clinical and regulatory documents to support clinical studies in a biotechnology company.