Explore 44 Remote Regulatory Documents Jobs
Lead clinical development initiatives for Myasthenia Gravis while supporting the APAC region in a remote role.
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Cogent Biosciences
Seeking an experienced medical writer to lead the development of clinical and regulatory documents in a biotechnology company.
Join PrimeVigilance as a Senior Medical Writer to lead a team and contribute to drug safety documentation.
The Senior Medical Writer will author and contribute to clinical and regulatory documents, ensuring compliance with ethical and regulatory standards.
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Dyne Therapeutics
The Associate Director, Medical Writing is responsible for preparing high-quality clinical and regulatory documents for Dyne Therapeutics.
The Medical Writing Coordinator/Publisher III manages document publishing and quality assurance for clinical and regulatory documents.
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Entrada Therapeutics
Entrada Therapeutics is seeking a Translational PK/PD Modeling Consultant to advance Ocular research and develop PK/PD models.
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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.
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Telix Pharmaceuticals (Americas)
The Medical Writer will lead the writing process for clinical and regulatory documents in a dynamic pharmaceutical company.
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Sidwell Company
Harris Healthcare is looking for a motivated Business Analyst to drive user stories and system requirements in healthcare software.
Excelya is seeking a Medical Writing Lead to coordinate clinical and regulatory documents in a collaborative environment.
The Project Management Specialist coordinates and supports clinical trials, ensuring regulatory compliance and effective communication across departments.
Join AbbVie as a Principal Strategic Medical Writer to lead and create high-quality clinical and regulatory documents.