Regulatory Affairs
Regulatory Affairs Coordinator
Resumé
The Regulatory Affairs Coordinator supports global regulatory operations, including eCTD submissions, regulatory publishing, document management and product life-cycle activities. The role may also contribute to Veeva RIMS implementation and ongoing development.
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Kort om jobbet
Global Regulatory Operations | eCTD Submissions | Regulatory Systems Job openings DeadlineOctober 24, 2026 DepartmentRegulatory Affairs Apply Pharmacosmos is seeking an experienced Regulatory Affairs Coordinator to join our Regulatory Affairs department of 21 employees. The department manages new marketing authorisation applications and the life-cycle management of human and veterinary medicinal products globally.
The role supports global regulatory operations, including eCTD submissions, regulatory publishing, document management and life-cycle activities across international markets. Experience with Veeva RIMS is preferred and may provide the opportunity to take on implementation and post-implementation responsibilities, depending on the candidate’s background.
Your responsibilities
Supporting global regulatory operations, including submission planning, document handling and regulatory follow-up - Contributing to Veeva RIMS implementation, maintenance, user support and continuous improvement, where relevant to your experience - Preparing, compiling, technically validating and submitting regulatory dossiers in eCTD format across1 …
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