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Pharmacovigilance Services Associate

1-3 years
Not Disclosed
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™.