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Senior Medical & Regulatory Writer – Clinical Research

Dicentra • Remote, US • published 2026-10-23 08:05:32.280262

Description

For over 25 years, dicentra has been a trusted global leader in regulatory consulting and clinical research for the life sciences and dietary supplement industries. We partner with innovators worldwide to navigate complex regulatory landscapes, turn scientific rigor into commercial success, and bring safe, compliant products to market. We have an immediate opening for an experienced Senior Medical \& Regulatory Writer to support the development of clinical and regulatory documentation across our clinical research portfolio. We welcome applications from professionals interested in full\-time or part\-time employment, as well as independent consultants available for project\-based or ad\-hoc assignments. **The Opportunity** In this role, you will lead the development of high\-quality clinical and regulatory documents supporting studies across pharmaceuticals, medical devices, and natural health products (NHPs) / dietary supplements. You will work collaboratively with clinical operations, biostatistics, regulatory specialists, and external partners to develop clear, scientifically accurate, and regulatory\-compliant documentation. This opportunity is ideal for an experienced medical w...

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