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Pharmacovigilance Services Associate

Accenture
Accenture
1-3 years
preferred by company
Bangalore, India
1 May 18, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding

Pharmacovigilance Services Associate

Location: Bengaluru, India
Job Type: Full-Time
Work Mode: Onsite / Rotational Shifts
Industry: Pharmacovigilance | Drug Safety | Life Sciences | Healthcare
Department: Pharmacovigilance Operations
Experience Required: 1–3 Years (Freshers May Be Considered for Entry-Level Openings Based on Business Requirements)
Qualification Required: Bachelor of Pharmacy (B.Pharm) / Master of Pharmacy (M.Pharm)
Job Reference ID: AIOC-S01645851
Employment Type: Individual Contributor

Job Overview

A leading global professional services organization is hiring a Pharmacovigilance Services Associate for its Bengaluru location. This opportunity is ideal for pharmacy professionals with experience in pharmacovigilance operations, drug safety surveillance, adverse event case processing, MedDRA coding, and regulatory safety reporting.

The selected candidate will support global pharmacovigilance operations involving Individual Case Safety Report (ICSR) case processing, adverse event data management, safety database documentation, follow-up activities, and compliance with international pharmacovigilance regulations.

This role is ideal for professionals looking to build or advance their careers in drug safety, pharmacovigilance operations, and regulatory healthcare services.

Job Responsibilities

Pharmacovigilance Operations

  • Support pharmacovigilance and drug safety surveillance activities for pharmaceutical products.
  • Monitor, assess, and process safety-related information according to client guidelines and global regulatory standards.
  • Ensure high-quality pharmacovigilance case management and reporting compliance.

ICSR Case Processing

Manage end-to-end Individual Case Safety Report (ICSR) activities including:

  • Case identification
  • Safety case intake
  • Data entry
  • MedDRA coding
  • Case triage
  • Case processing
  • Regulatory submission support
  • Follow-up case management
  • Safety database documentation

Drug Safety Surveillance

  • Monitor adverse event and drug safety data received from healthcare providers, patients, clinical programs, and other reporting sources.
  • Support evaluation of drug-related safety concerns.
  • Ensure timely pharmacovigilance reporting and compliance with global timelines.

Regulatory Compliance & Documentation

  • Follow pharmacovigilance SOPs, regulatory requirements, and client quality standards.
  • Maintain accurate documentation and audit-ready pharmacovigilance records.
  • Ensure compliance with internal quality and operational processes.

Team Collaboration

  • Work as an individual contributor within a structured pharmacovigilance operations team.
  • Collaborate with supervisors and internal stakeholders for daily task execution.
  • Resolve routine operational issues based on standard procedures and guidance.

Operational Requirements

  • Deliver assigned pharmacovigilance tasks within expected productivity and quality standards.
  • Adapt to rotational shift schedules based on operational requirements.
  • Support consistent delivery of safety operations services.

Educational Qualification

Candidates must have:

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

Preferred:

  • Pharmacovigilance certification
  • Drug safety operations training

Experience Requirements

  • 1–3 years of relevant experience in pharmacovigilance, drug safety, or healthcare operations
  • Prior experience in ICSR processing or safety operations preferred
  • Entry-level pharmacy professionals with relevant exposure may be considered depending on hiring requirements

Required Skills

  • Pharmacovigilance
  • Drug Safety Surveillance
  • ICSR Processing
  • Adverse Event Case Handling
  • MedDRA Coding
  • Safety Data Entry
  • Pharmacovigilance Operations
  • Regulatory Compliance
  • Safety Database Management
  • Drug Safety Documentation
  • Case Follow-Up Management
  • Life Sciences Operations
  • Quality Documentation
  • Communication Skills