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Pharmacovigilance Services Associate

0-2 years
Not Disclosed
10 Nov. 20, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Pharmacovigilance Services Associate – Bengaluru

Full-Time | Job No. AIOC-S01613990
Experience Required: 0–2 Years

Job Overview

The Pharmacovigilance Services Associate will support pharmacovigilance and drug safety surveillance activities, contributing to case processing, safety data management, and regulatory compliance for global life sciences and biopharmaceutical clients.


About the Role

This role is part of the Life Sciences R&D vertical, supporting end-to-end safety operations across clinical development, regulatory processes, pharmacovigilance, and patient safety services. You will help global biopharma organizations improve patient outcomes by ensuring high-quality safety reporting and adherence to international regulatory guidelines.


Key Responsibilities

  • Manage affiliate safety mailboxes, perform reconciliation of safety reports, and execute written follow-up activities for serious and non-serious cases.

  • Create and manage case identification, data entry, MedDRA coding, case processing, submission, and follow-up for ICSRs in compliance with client requirements and global regulatory standards.

  • Support internal safety operations as an individual contributor with a defined scope of work.

  • Solve routine operational issues using established guidelines and standard procedures.

  • Collaborate primarily with your team members and direct supervisor to ensure timely completion of assigned tasks.

  • Follow detailed instructions for new assignments and moderate guidance for daily activities.

  • Work in rotational shifts as required.


Experience Required

  • 0 to 2 years of experience in pharmacovigilance, drug safety, clinical research, or related life sciences operations.

  • Candidates with 1 to 3 years of prior experience are also eligible as per role expectations.

  • Familiarity with safety databases, MedDRA coding, and ICSR processing is preferred.


Minimum Qualifications

  • Bachelor of Pharmacy (B.Pharm) or Master of Pharmacy (M.Pharm).


Preferred Skills

  • Foundational understanding of pharmacovigilance operations and global drug safety regulations.

  • Basic knowledge of MedDRA terminology, case processing workflows, and regulatory timelines.

  • Ability to follow structured processes, adapt to rotational shifts, and maintain accuracy under timelines.


Location

  • Bengaluru, India