Join Clinical Research Courses and 100% job Assistance!
ChatJob description: Assisting in aggregated data reports preparation (periodic safety update reports (PSUR), addendum to clinical overview (ACO), risk management plans (RMPs). Maintain tracking systems and documentation for various pharmacovigilance processes and archiving as per Bluefish SOPs. Candidate Specifications Bachelor s degree in any life sciences or pharmaceutical sciences Knowledge in literature surveillance for pharmacovigilance activity is mandatory Excellent computer skills, including Word and Excel in a Microsoft Windows environment. Skills Abilities Requirements: Must have thorough knowledge of systems, processes and procedures related to pharmacovigilance, especially EU GVP
₹ 2.4 Lakhs to ₹ 6.8 Lakhs PA
Ipca Laboratories Limited is an Indian multinational pharmaceutical company based in Mumbai. It produces theobromine, acetylthiophene, and p-bromotoluene as active pharmaceutical ingredie...