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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: ICSR Case Processing, Interpersonal Skill, Labelling Assessment

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 Opportunities Based on Business Requirements)
Qualification Required: Bachelor of Pharmacy (B.Pharm) / Master of Pharmacy (M.Pharm)
Job Reference ID: AIOC-S01645850
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 seeking careers in pharmacovigilance, drug safety surveillance, adverse event processing, ICSR case management, MedDRA coding, and global regulatory safety operations.

The selected candidate will be responsible for supporting pharmacovigilance operations through accurate case intake, drug safety data management, adverse event processing, regulatory documentation, and compliance with international pharmacovigilance guidelines.

This is an excellent opportunity for early-career professionals looking to grow in pharmacovigilance and drug safety operations within the life sciences industry.

Job Responsibilities

Pharmacovigilance Operations

  • Support end-to-end pharmacovigilance and drug safety surveillance activities.
  • Monitor and process safety-related information according to client requirements and regulatory standards.
  • Ensure timely and compliant handling of drug safety operations.

ICSR Case Processing

Manage Individual Case Safety Report (ICSR) workflows including:

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

Drug Safety Surveillance

  • Monitor adverse event reports and drug-related safety information.
  • Support detection and evaluation of safety-related issues.
  • Ensure compliance with global pharmacovigilance reporting timelines and internal quality standards.

Regulatory Compliance & Documentation

  • Follow pharmacovigilance SOPs, client procedures, and international drug safety regulations.
  • Maintain accurate, complete, and audit-ready documentation.
  • Support quality compliance across pharmacovigilance workflows.

Team Collaboration

  • Work as an individual contributor within a structured operational team.
  • Collaborate with supervisors and internal teams to deliver assigned work.
  • Resolve routine process-related issues using standard operating guidelines.

Operational Requirements

  • Maintain productivity and quality expectations for assigned tasks.
  • Work in rotational shifts as per business requirements.
  • Adapt to process-driven healthcare operations environments.

Educational Qualification

Candidates must have:

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

Preferred:

  • Pharmacovigilance certification
  • Drug safety process exposure

Experience Requirements

  • 1–3 years of relevant experience in pharmacovigilance, drug safety, or healthcare operations
  • Experience in ICSR case processing preferred
  • Fresh pharmacy graduates with relevant training may be considered for suitable openings

Required Skills

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