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Pharmacovigilance Services Associate

0-2 years
Not Disclosed
10 Dec. 2, 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
Job Type: Full-Time
Experience: 0–2 years (Freshers eligible)
Location: Chennai, India
Job ID: AIOC-S01615295


About the Role

Accenture is hiring Pharmacovigilance Services Associates to support global Life Sciences and R&D operations. This role is part of the Clinical, Pharmacovigilance & Regulatory sub-offering under Accenture’s Life Sciences vertical, working with leading biopharmaceutical organizations to improve patient safety and regulatory compliance.

As a Pharmacovigilance Services Associate, you will perform case processing activities including case intake, MedDRA coding, data entry, follow-ups, and regulatory submissions for Individual Case Safety Reports (ICSRs). The position offers training, growth opportunities, and exposure to global PV processes.


Minimum Qualifications

  • Bachelor of Pharmacy (B.Pharm)

  • Master of Pharmacy (M.Pharm)


Experience Required

  • 0–2 years total experience

  • Candidates with 1–3 years PV experience preferred

  • Freshers with strong knowledge of pharmacovigilance basics may apply


Key Skills

  • Pharmacovigilance & Drug Safety Surveillance

  • Case processing and ICSR handling

  • Case identification and triaging

  • MedDRA coding

  • Data entry and database management

  • Written follow-up for Serious and Non-Serious cases

  • Knowledge of global regulatory requirements


Key Responsibilities

  • Manage affiliate mailbox and reconcile safety reports as per processes

  • Identify, create, and process ICSRs in the safety database

  • Perform MedDRA coding and ensure accurate case documentation

  • Conduct follow-ups and ensure timely submissions as per regulatory guidelines

  • Adhere to client-specific SOPs, timelines, and quality standards

  • Work as an individual contributor within a defined scope

  • Handle routine issues based on established guidelines

  • Work in coordination with supervisors and team members

  • Rotational shift work may be required


What You Will Do

You will be aligned with Accenture’s Life Sciences R&D vertical supporting:

  • Pharmacovigilance operations

  • Clinical research processes

  • Regulatory documentation activities

  • Patient safety initiatives for global biopharma clients


About Accenture

Accenture is a global professional services company with more than 775,000 employees, serving clients in over 120 countries. With deep capabilities across digital, cloud, operations, and strategy, Accenture is recognized as one of the World’s Best Workplaces™.
The company promotes diversity, inclusion, innovation, and people well-being, offering continuous learning, certifications, and career development opportunities.


Equal Employment Opportunity

Accenture is an equal opportunity employer. All employment decisions are free from discrimination based on age, race, color, religion, gender, sexual orientation, national origin, disability, marital status, or any legally protected category.


Fraud Alert

Accenture does not require payment at any stage of recruitment.
If you receive any payment request, report it to: india.fc.check@accenture.com