Internship in Pharmacovigilance

You will be responsible for performing various activities on behalf of the Marketing Authorization Holder. Your main responsibilities will include maintaining oversight of the Pharmacovigilance (PV) system in all relevant aspects, such as SOPs & Training, contractual arrangements, databases, compliance data, audit/inspection plans, PV systems of local affiliates, and ensuring that all PV processes are conducted in accordance with pertinent regulations. Additionally, you will oversee the preparation and maintenance of the PV System Master File, maintain an overview of safety profiles and any emerging safety concerns of all Marketing Authorization Holder products, manage the signal management process to identify possible safety signals, ensure awareness and appropriate fulfillment of CA queries and commitments, develop Risk Management Plans, and Periodic Safety Update Reports (PSUR). You will have input into the risk-based audit of the PV system, manage members of the QPPV Office, carry out continuous overall pharmacovigilance evaluation of the drug post-marketing, perform literature surveillance activity for all Marketing Authorization Holder products, and manage vendors for pharmacovigilance related work. This internship opportunity in Pharmacovigilance is for a duration of either 6 months or 1 year, and it is a paid internship. The salary will be as per company norms. The industry is Pharma/Biotech/Clinical Research, and the functional area includes Medical, Healthcare, R&D, Pharmaceuticals, and Biotechnology. The role category is Drug Regulatory Affairs/Documentation, and the specific role is Documentation/Medical Writing as an Intern. This position is an Intern to Hire employment type, and the qualification required is any Life Science graduate. If you are interested, you can forward your profile to contact@covalenttrainings.com or reach out for guidance at +91-9848733309 / +91-9676828080.,