Global Regulatory Submissions Lead

A biopharma company in Paris is seeking a Senior Consultant for Device Regulatory Documentation & Compliance. In this role, you will mentor a team, develop regulatory documentation, and ensure compliance for medical devices and combination products. This opportunity is perfect for someone with 5–7 years of experience in the field, a thorough understanding...

AXA Group Operations is seeking a Vendor Risk Regulatory Lead to manage regulatory obligations, data quality and vendor-risk governance across AXA entities. You will collaborate with Risk, Procurement, Legal and SMEs to ensure end‑to‑end source-to-contract processes meet regulatory requirements.The role focuses on DORA and Solvency II reporting,...

Syneos Health is seeking a Site Activation Manager for a sponsor-dedicated role based in Boulogne-Billancourt, near Paris.Maximisez vos chances de réussite pour cette candidature en vous assurant que votre CV et vos compétences correspondent bien.You will lead regulatory submissions, manage CTAs, and guide cross-functional teams through EU CTR processes to...

IQVIA is seeking a Principal Medical Writer in Paris to develop regulatory documents (IBs, CSRs, submission documents) for global regulatory authorities. You will lead and guide other writers, ensuring rigorous, data-accurate narratives across multiple compounds.Strong organizational and communication skills are essential for coordinating cross-functional...

Title: Regulatory Submission Project Manager Company: Ipsen Biopharm Ltd About Ipsen: Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology, Rare Disease and Neuroscience. Supported by nearly 100 years of development experience, with global hubs in the U.S., France and the U.K, we...

Design, implementation and coordination of clinical studies with the support of Clinical Operations, Pharmacovigilance, Biometrics and Medical Writing:Plan the clinical development programPrepare studies protocols, amendments and reportsPrepare regulatory dossiersManage relationships with investigators and opinion leadersRequirementsHolder of additional...

Ipsen is seeking an experienced CMC Regulatory Director to lead the regulatory strategy for assigned projects from development through lifecycle management. You will coordinate with Global Regulatory Affairs, Manufacturing, and external partners to ensure compliant CMC submissions and timely interactions with authorities.Ideal candidates will have 8–10...

En Carta Diagnostics in Paris is seeking a Senior Regulatory & Clinical Affairs Manager to own regulatory and clinical strategy for IVDR and FDA pathways, guiding products from technical file to market authorization.You will lead cross‑functional teams across biology, engineering and quality, build robust regulatory routes, and ensure timely, compliant...

You are looking for new challenges, you are passionate about procurement, regulations, vendor risk and thrilled to work within dynamic and international teams, come and join our AXA GO & GIE AXA Procurement Team.Postulez rapidement, consultez la description complète en faisant défiler la page ci-dessous pour découvrir toutes les exigences de ce...