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Pharmacovigilance Services Associate

Accenture
Accenture
0-2 years
preferred by company
Bangalore, India
1 May 14, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill

Pharmacovigilance Services Associate
Location: Bengaluru, Karnataka, India
Employment Type: Full-Time
Department: Pharmacovigilance / Drug Safety / Life Sciences R&D
Experience Required: 0–2 Years (Freshers with relevant pharmacy qualifications may be considered)


Job Overview

An excellent opportunity is available for a Pharmacovigilance Services Associate within the life sciences and drug safety domain. This role is ideal for candidates looking to build a career in pharmacovigilance operations, drug safety surveillance, adverse event reporting, ICSR processing, and global regulatory compliance.

The selected candidate will support pharmacovigilance activities focused on monitoring the safety of pharmaceutical products, identifying adverse drug reactions, processing safety cases, and ensuring compliance with global pharmacovigilance regulations and client quality standards.

This role is highly suitable for pharmacy graduates and early-career professionals seeking growth in drug safety, pharmacovigilance operations, clinical safety, and pharmaceutical regulatory services.


Key Responsibilities

Pharmacovigilance Operations

  • Support pharmacovigilance processes for monitoring pharmaceutical product safety
  • Identify, evaluate, and manage adverse drug reaction reports
  • Ensure compliance with client guidelines and global pharmacovigilance regulations
  • Contribute to patient safety monitoring and risk management initiatives

ICSR Case Processing

  • Perform case identification and intake for Individual Case Safety Reports (ICSRs)
  • Enter and validate safety data within pharmacovigilance databases
  • Manage complete ICSR lifecycle activities including:
    • Case intake
    • Data entry
    • MedDRA coding
    • Case processing
    • Case follow-ups
    • Safety submissions
  • Maintain accuracy, completeness, and regulatory timelines for case handling

Drug Safety Surveillance

  • Monitor drug safety signals and adverse event information
  • Assist in evaluating safety information collected from healthcare providers, clinical programs, and related reporting channels
  • Support high-quality safety documentation and reporting workflows

Operational Support

  • Resolve routine operational issues by following defined procedures and SOPs
  • Work closely with direct supervisors and pharmacovigilance teams
  • Deliver assigned safety tasks within required timelines
  • Maintain data quality and operational compliance standards

Required Qualifications

Educational Qualifications
Candidates should hold one of the following:

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

Preferred additional academic backgrounds:

  • PharmD
  • Life Sciences (if relevant pharmacovigilance exposure exists)

Required Skills & Competencies

  • Pharmacovigilance operations knowledge
  • Drug safety surveillance understanding
  • ICSR case processing awareness
  • Adverse event reporting knowledge
  • MedDRA coding familiarity
  • Pharmacovigilance database exposure
  • Strong analytical and problem-solving skills
  • Attention to detail and regulatory accuracy
  • Documentation and reporting skills
  • Strong communication and collaboration abilities
  • Ability to work in process-driven regulated environments