RemoteOtterRemoteOtterExplore 40 Remote Regulatory Documents Jobs
D.T
Dyne Therapeutics
The Associate Director, Medical Writing is responsible for preparing high-quality clinical and regulatory documents for Dyne Therapeutics.
AbbVie
The Medical Writing Coordinator/Publisher III manages document publishing and quality assurance for clinical and regulatory documents.
E.T
Entrada Therapeutics
Entrada Therapeutics is seeking a Translational PK/PD Modeling Consultant to advance Ocular research and develop PK/PD models.
E.L.C
Eli Lilly Canada
Join Lilly as a Clinical Development Scientist to manage clinical supplies and support global clinical programs in gene therapy.
Neumora
Neumora
Seeking a Senior Director/Director, Clinical Scientist to lead scientific expertise in drug product development at Neumora.
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.
Excelya
Excelya is seeking a Medical Writing Lead to coordinate clinical and regulatory documents in a collaborative environment.
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.