Instagram
youtube
Facebook

Pharmacovigilance Services Associate

2+ years
Not Disclosed
10 Oct. 30, 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

Job Title

Pharmacovigilance Services Associate


Job Details

  • Job ID: AIOC-S01610388

  • Location: Bengaluru, India

  • Employment Type: Full Time

  • Experience Required: 0–2 years (preferred: 1–3 years)

  • Qualification: Bachelor of Pharmacy (B.Pharm) / Master of Pharmacy (M.Pharm)

  • Department: Pharmacovigilance Operations – Drug Safety Surveillance

  • Company: Accenture


About Accenture

Accenture is a global professional services company with leading capabilities in digital, cloud, and security.
With 699,000+ employees across 120+ countries, Accenture delivers Strategy & Consulting, Technology, Operations, and Accenture Song services, all powered by the world’s largest network of Advanced Technology and Intelligent Operations centers.
Visit: www.accenture.com


Job Overview

As a Pharmacovigilance Services Associate, you will be aligned with the Life Sciences R&D vertical, focusing on Pharmacovigilance & Drug Safety Surveillance.
You will support global biopharma clients by ensuring accurate safety data collection, processing, and regulatory compliance in alignment with ICH-GCP and global safety standards.


Key Responsibilities

  • Manage Affiliate Mailbox and perform reconciliation of reports as per process.

  • Conduct written follow-up for both serious and non-serious adverse event (AE) cases.

  • Create, identify, and manage safety cases (ICSRs) in the safety database.

  • Perform data entry, MedDRA coding, case processing, submission, and follow-up as per client and regulatory guidelines.

  • Ensure compliance with global regulatory requirements for pharmacovigilance.

  • Collaborate effectively with team members and supervisors.

  • Work in rotational shifts as required.


Required Skills

  • Strong understanding of pharmacovigilance processes and drug safety surveillance.

  • Knowledge of MedDRA coding and safety databases.

  • Attention to detail and accuracy in safety data handling.

  • Good communication and teamwork skills.

  • Ability to follow SOPs and global regulatory guidelines.


Desired Profile

  • Freshers or candidates with up to 2 years of PV experience are eligible.

  • Strong knowledge of pharmacovigilance, GVP, and regulatory frameworks.

  • Willingness to work in rotational shifts.


Equal Employment Opportunity

Accenture provides equal employment opportunities to all qualified applicants without discrimination based on age, gender, race, religion, disability, or any other protected status.
Read more in Accenture’s Recruiting and Hiring Statement.


Important Notice (Fraud Alert)

Accenture never requires payment from candidates during hiring.
If you receive any communication requesting payment, report it immediately to:
📧 india.fc.check@accenture.com


Company Values

  • Purpose: Deliver on the promise of technology and human ingenuity.

  • Culture: Inclusive, diverse, and innovation-driven.

  • Well-being: Holistic focus on physical, mental, and financial health.

  • Growth: Continuous learning, certification, and career development opportunities.


✅ Apply Now: Accenture Careers