Pharmacovigilance Associate

About the role - Join a life sciences drug safety monitoring team as a full-time, entry-level Pharmacovigilance Associate. - This opportunity is open to fresh graduates and candidates with up to 1 year of experience, offering structured training and hands-on exposure to global safety surveillance and regulatory compliance. Key responsibilities - Process Individual Case Safety Reports (ICSRs) for adverse events in accordance with standard operating procedures. - Perform MedDRA coding of adverse event terms and patient medical history. - Enter, verify and maintain safety data in pharmacovigilance databases. - Assist with literature screening, signal detection reviews and safety data analysis. - Support preparation of Periodic Safety Update Reports (PSURs) and Periodic Benefit-Risk Evaluation Reports (PBRERs). - Maintain compliance with Good Pharmacovigilance Practices (GVP) and regulatory guidelines. What we offer - Comprehensive on-the-job training. - Clear career progression within drug safety and regulatory affairs. - Collaborative and supportive work culture.