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Pharmacovigilance Services Analyst

Accenture
Accenture
2-5 years
preferred by company
10 Jan. 6, 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, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Pharmacovigilance Services Analyst

Location: Chennai, India
Employment Type: Full-Time
Industry: Pharmacovigilance | Drug Safety | Life Sciences
Experience Required: 2–5 Years
Job ID: AIOC-S01620520
Company: Accenture


Role Overview

Accenture is hiring a Pharmacovigilance Services Analyst to support global drug safety and pharmacovigilance operations within its Life Sciences R&D vertical. This role focuses on individual case safety report (ICSR) processing, safety database management, and compliance with global regulatory requirements.

The position is ideal for professionals with hands-on experience in pharmacovigilance case processing, MedDRA coding, and safety reporting, along with basic proficiency in the Japanese language.


Key Responsibilities

Pharmacovigilance & Drug Safety Operations

  • Perform case intake, identification, and data entry for ICSRs

  • Conduct MedDRA coding, case processing, and quality review

  • Manage case submissions and follow-ups in safety databases as per client SOPs

  • Ensure compliance with global pharmacovigilance regulations and timelines

Regulatory & Compliance Support

  • Support safety surveillance activities aligned with international regulatory requirements

  • Maintain accurate documentation and audit-ready records

  • Follow established pharmacovigilance processes and quality standards

Collaboration & Reporting

  • Work closely with team members and supervisors on daily operational activities

  • Provide timely status updates and escalate issues when required

  • Operate as an individual contributor within a structured team environment


Required Qualifications & Experience

  • Education: Any Graduation / Bachelor of Pharmacy / Master of Pharmacy

  • Experience: 2 to 5 years of relevant experience in Pharmacovigilance or Drug Safety

  • Language Skills:

    • Japanese – Elementary proficiency

    • JLPT certification N3 to N5 preferred


Desired Skills & Competencies

  • Strong understanding of pharmacovigilance case processing and ICSR workflows

  • Familiarity with safety databases and MedDRA terminology

  • Ability to analyze and resolve low to moderate complexity issues

  • Adaptable, flexible, and quick learner in a dynamic environment

  • Strong teamwork, coordination, and communication skills


Role Characteristics

  • Individual contributor role with a focused scope of work

  • Limited direct client exposure

  • Moderate supervision with detailed guidance on new assignments

  • May require working in rotational shifts

  • Decisions impact personal work deliverables and team outcomes


About Accenture

Accenture is a global professional services company with leading capabilities in digital, cloud, security, and life sciences operations. With a workforce of over 699,000 professionals across 120+ countries, Accenture helps the world’s leading biopharma and healthcare organizations improve patient outcomes through innovation, compliance, and operational excellence.


Why Apply Through ThePharmaDaily.com

  • Verified global life sciences and pharmacovigilance roles

  • Trusted platform for PV, Drug Safety, Clinical Research, and Regulatory Affairs jobs

  • Career opportunities with top pharmaceutical and healthcare organizations

Apply now to advance your pharmacovigilance career with Accenture in Chennai.