Novo Nordisk is a global healthcare company with 89 years of innovation and leadership in diabetes care. The company also has leading positions within Haemophilia care, growth hormone therapy and hormone replacement therapy.
Post : Jr Assoc Pharmocovigilance
Job Description
As Jr Assoc Pharmacovigilance, you will help make sure safety information reaches the right people at the right time. You will process adverse events and product quality complaints, support timely reporting to local Health Authorities and keep safety records accurate and inspection-ready. Working in International Operations, you will turn every report into reliable data that supports people using Novo treatments and strengthens pharmacovigilance operations.
What you’ll do
You will be part of the local safety process from first report to closure, working under appropriate supervision while building your own expertise.
• Receive, document and report adverse events (AEs), product quality complaints (PQCs) and AEs associated with PQCs to Global Safety within required timelines, including follow-up until closure.
• Monitor the safety mailbox and handle safety information and customer complaints received by phone, through digital applications and via internal safety portals.
• Carry out assigned activities across the ICSR lifecycle in Veeva Safety and Veeva Quality, from intake, assessment and case narrative preparation to quality review, submission, follow-up and closure.
• Perform quality checks, source data verification and reconciliations, so cases are accurate, complete and consistent.
• Support the preparation, submission and tracking of clinical trial safety reports (including SUSARs and SAEs) and post-marketing ICSRs to Health Authorities.
• Maintain safety databases, submission trackers and pharmacovigilance records, and keep documentation complete and retrievable for audits and inspections.
• Support monitoring of local PV requirements, flag new or amended requirements to Global Safety, and help track compliance activities, escalating potential delays or issues early.
Candidate Profile
• A bachelor’s degree in pharmacy, A Master’s degree (M. Pharm or PharmD) is preferred.
• Training in pharmacovigilance basics or safety databases is preferred. If you have experience, 1–2 years in pharmacovigilance or drug safety is what we are looking for.
• A basic understanding of pharmacovigilance processes, adverse event reporting and ICSR processing, and of regulatory guidelines such as ICH, the New Drugs and Clinical Trials Rules 2019 (NDCT), Pharmacovigilance Programme of India (PvPI) guidelines and applicable Good Pharmacovigilance Practices (GVP).
• Good written and verbal communication, strong attention to detail and solid documentation skills.
• Familiarity with Veeva Safety or Veeva Quality.
• The ability to prioritise tasks, meet timelines, work collaboratively and escalate issues promptly.
• Proficiency in Microsoft Office applications.
• Fluency in English.
Additional Information
Experience : 1–2 years
Qualification : B.Pharm, M.Pharm, PharmD
Location : Bangalore, Karnataka
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Pharmacovigilance
End Date : 10th December 2026
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