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Pharmacovigilance Services New Associate

Accenture
Accenture
0-1 years
Not Disclosed
Bengaluru, India
10 April 14, 2026
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Pharmacovigilance Services New Associate – Bengaluru | Drug Safety | Pharma Jobs

Company: Accenture
Location: Bengaluru, India
Job Type: Full-Time
Work Mode: Not Specified
Experience: 0–1 Year
Qualification: MSc / B.Pharm / M.Pharm


Job Overview

This role focuses on pharmacovigilance operations and drug safety surveillance within the life sciences domain. The position involves monitoring adverse events, processing safety data, and ensuring compliance with global regulatory requirements to maintain the safety of pharmaceutical products.


Key Responsibilities

Pharmacovigilance Operations

  • Perform case identification, data entry, and case processing for ICSRs
  • Conduct MedDRA coding for adverse events and medical data
  • Manage safety data within global safety databases

Drug Safety & Surveillance

  • Monitor and evaluate adverse drug reactions and safety signals
  • Support detection, assessment, and prevention of drug-related risks
  • Ensure compliance with pharmacovigilance guidelines and regulations

Case Processing & Submission

  • Handle end-to-end ICSR processing including follow-ups
  • Ensure timely submission of safety reports as per regulatory timelines
  • Maintain data accuracy and completeness in safety systems

Required Skills & Qualifications

Education

  • MSc / Bachelor of Pharmacy / Master of Pharmacy

Experience

  • 0–1 year of relevant experience

Technical Skills

  • Basic knowledge of pharmacovigilance and drug safety processes
  • Familiarity with MedDRA coding and safety databases (preferred)
  • Working knowledge of MS Office tools

Core Competencies

  • Attention to detail and accuracy
  • Understanding of pharmacovigilance processes
  • Ability to follow SOPs and regulatory guidelines
  • Analytical and problem-solving skills
  • Team collaboration and communication

Perks & Benefits

  • Opportunity to work in global pharmacovigilance operations
  • Exposure to drug safety and regulatory compliance processes
  • Structured learning and career growth opportunities
  • Collaborative and process-driven work environment

About the Role

This role is ideal for entry-level professionals looking to build a career in pharmacovigilance. It provides hands-on experience in drug safety case processing, regulatory compliance, and global safety database management within a structured environment.


Salary / Compensation

💰 Not Disclosed (Competitive Package Expected)


Work Mode

📍 Bengaluru, India (Work mode not specified; rotational shifts may apply)