ProductLife Group is looking for a Case Specialist (Pharmacovigilance) to join our dynamic team to contribute to the activities performed in the Hub: Role:Responsible for the Quality control of vigilance casesMedical evaluation of reportsData entry of vigilance cases in ad hoc databases or in other formats agreed with the clientFollow-up request of vigilance cases by phone/mailPre-analysis of complex cases prior to data entryMedical evaluation of files on:Coding (according to applicable dictionary)Causal relationship between the effects and the intake of suspect products (according to applicable method)The expected/listed or unlisted nature of the events/effects/incidentsThe seriousness of the events/effects/incidents and the caseIdentification of submission requirements for each caseValidation of certain documents produced by the Data Manager/ Vigilance Associate / documentalist (phone call forms, etc)Closing of vigilance filesIdentification of requirements and applicable changes to set up ICSR/MLM filtersAnalysis of inclusion / exclusion of EV/MHRA casesMedical information in support of the medical information divisionRelated to particular activities carried out in their Business unit for specific clients Education & ExperienceDoctor or pharmacist by trainingMinimum 4 years experience working for service providers performing QC of caseSafetyEasy/ Argus database experience ProfileDatabase experience preferredKnowledge of current regulationsProcess orientedRigorous and ability to work in a teamUse of Microsoft Office toolsAbility to multitaskFlexibilityExcellent communication skills in English and French for business continuity