Pharmacovigilance Services Associate

1-3 years

Not Disclosed

Bengaluru

10 Oct. 9, 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 No.: AIOC-S01608227
💼 Employment Type: Full-time
🎓 Qualification: Bachelor of Pharmacy (B.Pharm)
🧭 Experience: 0–2 years (Preferred: 1–3 years)

About Accenture

Accenture is a global professional services company with leading capabilities in digital, cloud, and security.
With unmatched experience and specialized skills across 40+ industries, we offer:

Strategy & Consulting
Technology & Operations
Accenture Song

Our 775,000+ people deliver on the promise of technology and human ingenuity, serving clients in over 120 countries.
We believe in innovation through inclusion — fostering an environment where everyone feels valued, supported, and inspired to do their best work.

🌐 Visit: www.accenture.com

Role Overview

As a Pharmacovigilance Services Associate, you will support Life Sciences R&D functions, primarily focusing on Pharmacovigilance & Drug Safety Surveillance.
You will handle end-to-end Individual Case Safety Reports (ICSRs), including data entry, MedDRA coding, follow-ups, and submissions as per client and regulatory guidelines.

Key Responsibilities

Manage Affiliate Mailbox and ensure reconciliation of safety reports per process.
Perform case identification, data entry, MedDRA coding, and case processing in the safety database.
Handle serious and non-serious adverse event follow-ups per global regulatory requirements.
Create and manage case submissions according to client-specific and global pharmacovigilance standards.
Collaborate with internal team members and supervisors to ensure compliance and data quality.
Ensure timely and accurate documentation in line with applicable SOPs and client expectations.
Work in rotational shifts as required.

Skills & Competencies

Strong understanding of Pharmacovigilance & Drug Safety processes.
Knowledge of global regulatory guidelines (e.g., ICH, EMA, FDA).
Attention to detail and data accuracy.
Good communication and documentation skills.
Ability to follow structured workflows and standard procedures.
Team-oriented mindset and adaptability to rotational work schedules.

Work Environment

You will work as an individual contributor within a team structure.
Decisions made will primarily impact your own deliverables.
Guidance and supervision will be provided, especially for new or complex tasks.
Routine problem-solving through existing precedents and guidelines.

Equal Employment Opportunity Statement

Accenture is an Equal Opportunity Employer.
All employment decisions are made without regard to:
age, race, color, religion, creed, sex, national origin, ancestry, disability, veteran status, sexual orientation, gender identity or expression, marital status, genetic information, or any other protected status under law.

🔒 Please review Accenture’s Recruiting and Hiring Statement to understand how your data is processed during recruitment.

Important Notice (Fraud Alert)

🚫 Accenture does not charge any fees at any stage of the recruitment process.
If you are contacted by anyone requesting payment for employment opportunities, do not respond.
📩 Report such incidents to: india.fc.check@accenture.com

Why Join Accenture?

✅ Work at the heart of innovation and transformation.
✅ Continuous learning, certification, and skill development opportunities.
✅ Support for physical, mental, and financial well-being.
✅ Recognized globally as one of the World’s Best Workplaces™.

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Pharmacovigilance Services Associate

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