Instagram
youtube
Facebook

Pharmacovigilance Services Associate

1-3 years
Not Disclosed
10 Sept. 8, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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 Associate

Company: Accenture
Location: Bengaluru, India
Job Type: Full-time
Experience Required: 1–3 years
Qualification: Bachelor of Pharmacy (B.Pharm) / Master of Pharmacy (M.Pharm)
Skill Area: Pharmacovigilance Operations – Pharmacovigilance & Drug Safety Surveillance


About Accenture

Accenture is a global professional services company with leading expertise in digital, cloud, and security. With more than 775,000 employees across 120+ countries, we combine deep industry knowledge and specialized skills to deliver:

  • Strategy & Consulting

  • Technology & Operations Services

  • Accenture Song

Our Life Sciences R&D vertical supports research laboratories, clinical trials, regulatory services, pharmacovigilance, and patient solutions—helping leading biopharma companies improve outcomes and connect science with patient needs.

Visit us at www.accenture.com


Role Overview

As a Pharmacovigilance Services Associate, you will support pharmacovigilance and patient safety activities for global biopharma clients. This includes managing case intake, safety data entry, regulatory submissions, and follow-ups for Individual Case Safety Reports (ICSRs).


Key Responsibilities

  • Manage Affiliate Mailbox and reconcile safety reports.

  • Perform written follow-up attempts for both serious and non-serious cases.

  • Handle case identification, data entry, MedDRA coding, processing, submission, and follow-ups in the safety database.

  • Ensure compliance with client guidelines and global regulatory requirements.

  • Solve routine problems using general guidelines and precedents.

  • Interact primarily with your team and direct supervisor.

  • Work as an individual contributor with a focused scope of work.

  • Follow detailed instructions for daily tasks and new assignments.

  • Role may require working in rotational shifts.


Candidate Profile

  • Education: B.Pharm or M.Pharm.

  • Experience: 1–3 years in pharmacovigilance or drug safety.

  • Skills:

    • Strong knowledge of pharmacovigilance operations.

    • Good organizational and communication skills.

    • Ability to follow detailed processes accurately.

    • Willingness to work in shifts.


Equal Employment Opportunity

Accenture is an equal opportunity employer. Employment decisions are made without regard to:
Age, race, creed, color, religion, sex, national origin, ancestry, disability status, veteran status, sexual orientation, gender identity/expression, genetic information, marital status, citizenship, or any other protected category under applicable law.


Why Join Accenture?

  • Work with world-leading clients in biopharma and life sciences.

  • Opportunities to upskill through certifications, learning programs, and diverse work experiences.

  • Focus on well-being: physical, mental, and financial.

  • Inclusive, bias-free workplace where everyone is respected and empowered.

  • Recognized as one of the World’s Best Workplaces™.


Important Notice

⚠️ Accenture never asks job seekers to pay any fees related to employment. If you are contacted by someone requesting payment, do not respond. Report immediately to: india.fc.check@accenture.com.


Join Accenture and be at the heart of change.