Case Specialist- Pharmacovigilance

Case Specialist (Pharmacovigilance) • ProductLife Group • Canton of Montauban-1, France Base pay range The base pay range is provided by ProductLife Group. Your actual pay will be based on your skills and experience—talk with your recruiter to learn more. Responsibilities Responsible for the quality control of vigilance cases Medical evaluation of reports Data entry of vigilance cases in ad hoc databases or other formats agreed with the client Follow‑up request of vigilance cases by phone/mail Pre‑analysis of complex cases prior to data entry Medical evaluation of files on coding (according to applicable dictionary) Medical evaluation of files on causal relationship between the effects and the intake of suspect products (according to applicable method) Medical evaluation of files on the expected/listed or unlisted nature of the events/effects/incidents Medical evaluation of files on the seriousness of the events/effects/incidents and the case Identification of submission requirements for each case Validation of certain documents produced by the Data Manager/Vigilance Associate/documentalist (phone call forms, etc.) Closing of vigilance files Identification of requirements and applicable changes to set up ICSR/MLM filters Analysis of inclusion / exclusion of EV/MHRA cases Medical information in support of the medical information division Related to particular activities carried out in their Business unit for specific clients Education & Experience Doctor or pharmacist by training Minimum 3 years experience working for service providers performing QC of case SafetyEasy database experience Profile Database experience preferred Knowledge of current regulations Process oriented Rigorous and ability to work in a team Use of Microsoft Office tools Ability to multitask Flexibility Excellent communication skills in English and French for business continuity Seniority level Associate Employment type Full‑time Job function Legal Industries Pharmaceutical Manufacturing #J-18808-Ljbffr