Regulatory Medical Writer

ResponsibilitiesMedical writing of all types of regulatory and clinical study documentation including Investigators’ Brochures, clinical study reports and protocolsPreparation of regulatory responses to health authoritiesPreparation of marketing authorisation applications (eCTD module 2)Simultaneously manage several projects and meet tight...

DescriptionEn tant que Responsable Affaires Réglementaires & Senior Medical Writer, vous jouerez un rôle clé dans la coordination de la conformité réglementaire et la production de documents scientifiques de haute qualité pour accompagner le développement de nos produits.Intégré(e) au sein de l’équipe Affaires Réglementaires et Communication...

DescriptionEn tant que Responsable Affaires Réglementaires & Senior Medical Writer, vous jouerez un rôle clé dans la coordination de la conformité réglementaire et la production de documents scientifiques de haute qualité pour accompagner le développement de nos produits. Intégré(e) au sein de l’équipe Affaires Réglementaires et Communication...

## Senior Regulatory Affairs SpecialistApplylocations: Paris, Francetime type: Full timeposted on: Posted Todayjob requisition id: R1556847**Shape the future of regulatory excellence at IQVIA**At IQVIA, we work to advance healthcare by helping our clients bring safe, effective medicines to patients. As a Senior Regulatory Affairs Specialist, you will...

Raidium is seeking a Head of QARA to define our regulatory strategy and ensure AI-native solutions meet safety and quality standards. You will lead global MDR/FDA submissions and coordinate technical files, clinical data, and audits.You will mentor a junior QARA, maintain the QMS, and collaborate with R&D and Product to embed Compliance by Design into our...

Manager, Regulatory Affairs - EMEA- Remote page is loaded## Manager, Regulatory Affairs - EMEA- Remoteremote type: Remotelocations: Bucuresti, Romanina: Paris, France: Virtual Croatia: Madrid, Spain: England, United Kingdomtime type: Full timeposted on: Posted Todayjob requisition id: JR102988**Who we are**We're a global, midsize CRO that pushes boundaries,...

Associate Director, Regulatory & Pharmaceutical Affairs (Chief Pharmaceutical Officer Deputy)Paris, FranceThis senior pharmaceutical and regulatory position acts as the trusted right-hand partner (“bras droit”) to the Responsible Pharmacist (RP)/Chief Pharmaceutical Officer (CPO). Working in very close collaboration with the RP/CPO, the role supports the...

Making preventive health the default for every human in Europe The mission At Lucis, we believe healthcare should be preventive, not reactive. We’re building the operating system for human longevity to help people add more healthy years to their lives. The role Lucis analyses 110+ biomarkers, builds personalised clinical protocols, and delivers them...

Ipsen Pharma (SAS) is seeking a Medical Event Project Manager to lead and orchestrate global medical events, coordinating cross-functional teams to turn strategic objectives into compliant, cost-conscious execution. You will manage logistics, vendors, and budgets while upholding ethics and regulatory standards.The role requires a BA diploma and...