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Pharmacovigilance Services Analyst – Accenture

Accenture
3-5 years
Not Disclosed
Bangalore, India
2 May 20, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing

Pharmacovigilance Services Analyst – Accenture

Company: Accenture
Role: Pharmacovigilance Services Analyst
Location: Bengaluru, India
Job Type: Full-time
Experience Required: 3–5 Years (header mentions 2–5 years, detailed JD specifies 3–5 years)
Qualification: Bachelor of Pharmacy (B.Pharm) / Master of Pharmacy (M.Pharm)
Job ID: AIOC-S01645846

About Accenture

Accenture is a global professional services company providing consulting, technology, digital, cloud, and operations services across industries including life sciences and healthcare.

Job Overview

Accenture is hiring a Pharmacovigilance Services Analyst under its Life Sciences R&D vertical. This role focuses on drug safety surveillance, adverse event case processing, MedDRA coding, ICSR management, and pharmacovigilance operations to support global biopharma clients.

Key Responsibilities

  • Perform pharmacovigilance case processing activities
  • Create, review, and manage Individual Case Safety Reports (ICSRs)
  • Case identification and triage
  • Safety data entry into pharmacovigilance databases
  • Perform MedDRA coding for adverse events
  • Conduct follow-ups for incomplete safety cases
  • Ensure timely regulatory submissions per global requirements
  • Review adverse event reports from multiple sources:
    • Clinical trials
    • Healthcare professionals
    • Patients
    • Literature / safety sources
  • Maintain compliance with client SOPs and regulatory guidelines
  • Support drug safety surveillance and signal monitoring activities
  • Work in rotational shifts if required

Required Skills

  • Pharmacovigilance Operations
  • Drug Safety Surveillance
  • ICSR Processing
  • Adverse Event Case Processing
  • MedDRA Coding
  • Safety Database Management
  • Regulatory Compliance
  • Case Triage
  • Follow-up Management
  • Data Entry & Quality Review
  • Global PV Regulations
  • Clinical Safety Documentation

Domain Knowledge Required

Strong understanding of:

  • Pharmacovigilance workflows
  • Adverse Event (AE) reporting
  • Serious Adverse Event (SAE) handling
  • ICSR lifecycle management
  • Drug safety databases
  • Regulatory reporting timelines
  • Life Sciences / Biopharma industry processes

Soft Skills

  • Analytical thinking
  • Problem-solving
  • Attention to detail
  • Team collaboration
  • Communication skills
  • Time management
  • Process compliance
  • Ability to work in rotational shifts