Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Pharmacovigilance Services Associate

Accenture
Accenture
0-3 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: Environment, Experiments Design, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, Sop (Standard Operating Procedure), Technical Writing, Wat, GCP guidelines, gmp knowledge, HSE Knowledge , Logistics and Transportation Management, Master Data, Operational Excellence, Sap Erp, supply chain management, Supply Planning, Warehouse Management, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines

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: 0–3 Years (Freshers Eligible for Entry-Level Pharmacovigilance Roles)
Qualification Required: Bachelor of Pharmacy (B.Pharm) / Master of Pharmacy (M.Pharm)
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 interested in building a career in pharmacovigilance, drug safety surveillance, adverse event case processing, and global regulatory safety operations.

The selected candidate will support pharmacovigilance operations involving Individual Case Safety Report (ICSR) processing, case intake, safety data entry, MedDRA coding, follow-up management, and regulatory safety compliance.

This is an excellent opportunity for entry-level and early-career professionals seeking growth in pharmacovigilance, drug safety, and life sciences operations.

Key Responsibilities

Pharmacovigilance Operations

  • Support pharmacovigilance and drug safety surveillance activities for pharmaceutical products.
  • Monitor and process drug safety information in accordance with client requirements and global regulatory guidelines.
  • Ensure accurate and timely pharmacovigilance case handling.

ICSR Case Processing

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

  • Case identification
  • Safety data entry
  • Case triage
  • MedDRA coding
  • Case processing
  • Case follow-ups
  • Regulatory submission support
  • Safety database documentation

Drug Safety Surveillance

  • Monitor adverse event reports and drug safety information from multiple sources.
  • Support evaluation of potential drug safety concerns.
  • Ensure compliance with pharmacovigilance reporting timelines and quality standards.

Regulatory Compliance

  • Follow pharmacovigilance SOPs, client guidelines, and global drug safety regulations.
  • Maintain high-quality documentation standards for safety reporting activities.
  • Ensure accurate handling of safety information in compliance-driven environments.

Team Collaboration

  • Work closely with team members, supervisors, and internal stakeholders.
  • Participate as an individual contributor within a structured pharmacovigilance operations team.
  • Support assigned daily operational tasks with accuracy and consistency.

Operational Responsibilities

  • Solve routine pharmacovigilance workflow issues based on defined procedures and internal guidance.
  • Manage assigned work within agreed productivity and quality expectations.
  • Adapt to rotational shifts based on business requirements.

Educational Qualification

Candidates must have:

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

Preferred:

  • Pharmacovigilance certification
  • Drug safety training exposure

Experience Requirements

  • 0–3 years of relevant experience in pharmacovigilance, drug safety, or healthcare operations
  • Freshers with pharmacy backgrounds may apply for entry-level opportunities
  • Prior ICSR processing experience will be an added advantage

Required Skills

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