RIM Expert

ContextReplacement position (retirement)Supporting multiple clients across EuropeStart date: First half of 2026Permanent positionKey ResponsibilitiesProvide RIM expertise and consulting to clientsLead and support RIM implementation projectsAdvise clients on IDMP compliance and xEVMPDManage regulatory data and systemsAct as a project leader and coordinate stakeholdersContribute to IT and regulatory system integrationProfile RequiredBackground in Life Sciences or IT5 10 years of experience in Regulatory Affairs / RIMExperience in the pharmaceutical industry is a strong plusTechnical SkillsStrong expertise in Veeva Vault RIM / Ennov RIMKnowledge of IDMP & xEVMPD standardsAdvanced Excel skills (Power Query)LanguagesEnglish requiredFrench is a plusSoft SkillsAutonomous and organizedStrong analytical and problem-solving skillsAbility to lead projects and manage prioritiesAdaptable with a client-oriented mindsetWork SetupBased in EuropeRemote possible, but requires travel to client sites