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 Analyst

Accenture
Accenture
2-5 years
Not Disclosed
Bengaluru, India
9 April 24, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing

PHARMACOVIGILANCE SERVICES ANALYST | LIFE SCIENCES DRUG SAFETY OPERATIONS | ACCENTURE | BENGALURU

JOB OVERVIEW
The Pharmacovigilance Services Analyst role at Accenture is a mid-level position within Life Sciences Pharmacovigilance Operations. The role focuses on drug safety surveillance, case processing, and regulatory compliance activities that ensure the safety and effectiveness of pharmaceutical products across global markets.

The position supports leading biopharmaceutical clients by managing adverse event data, regulatory case reporting, and pharmacovigilance database operations aligned with global safety standards.

JOB TYPE
Full-Time | Individual Contributor Role | Rotational Shifts Applicable

LOCATION
Bengaluru, India

EXPERIENCE REQUIRED
2 to 5 years of experience in Pharmacovigilance / Drug Safety Operations

QUALIFICATION REQUIRED
MSc / Bachelor of Pharmacy (B.Pharm) / Master of Pharmacy (M.Pharm)

FUNCTION AREA
Life Sciences R&D | Pharmacovigilance Operations | Drug Safety Surveillance

KEY RESPONSIBILITIES

  • Perform pharmacovigilance case processing including data entry and case validation

  • Manage Individual Case Safety Reports (ICSRs) in safety databases as per regulatory requirements

  • Conduct MedDRA coding and ensure accurate classification of adverse event data

  • Support case identification, follow-ups, and reconciliation activities

  • Ensure compliance with global pharmacovigilance guidelines and client-specific SOPs

  • Monitor and evaluate adverse drug reactions from clinical and post-marketing data sources

  • Support regulatory reporting timelines for safety submissions

  • Collaborate with internal teams for data validation and quality checks

  • Maintain accuracy and completeness of pharmacovigilance documentation

  • Assist in continuous improvement of drug safety processes and reporting systems

SKILLS AND COMPETENCIES REQUIRED

  • Strong understanding of Pharmacovigilance and Drug Safety processes

  • Knowledge of MedDRA coding and ICSR case processing

  • Analytical and problem-solving abilities for structured data evaluation

  • Familiarity with global pharmacovigilance regulations and compliance frameworks

  • Ability to work with safety databases and reporting tools

  • Attention to detail and strong documentation skills

  • Ability to work in a structured, process-driven environment

  • Willingness to work in rotational shifts

  • Effective teamwork and communication skills

ROLE EXPECTATIONS

  • Works as an individual contributor within a supervised team structure

  • Handles moderate-complexity pharmacovigilance cases

  • Limited client interaction with primary focus on internal coordination

  • Follows detailed instructions for new assignments and SOP-driven tasks

  • Decisions primarily impact individual work output and team processes

ABOUT THE ORGANIZATION
Accenture is a global professional services organization operating across more than 120 countries. The company provides services in Strategy & Consulting, Technology, Operations, and Digital Transformation. Within Life Sciences, Accenture supports pharmaceutical and biotechnology companies in pharmacovigilance, clinical research, and regulatory operations to improve patient safety and healthcare outcomes.

NOTE
This role follows a strict ethical hiring process. Candidates are not required to make any payments at any stage of recruitment. All applications are evaluated based on merit and eligibility criteria.