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Pharmacovigilance Services Associate

1-3 years
₹3.5 – 6 LPA
10 Aug. 21, 2025
Job Description
Job Type: Full Time Education: B.Pharm/M.Pharm 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 – Accenture
Location: Mumbai, India
Job No.: AIOC-S01593590
Estimated Salary: ₹3.5 – 6 LPA (based on industry averages for entry-level pharmacovigilance roles in India)
Experience Required: 0–2 years
Employment Type: Full-time


About the Role

As a Pharmacovigilance Services Associate, you will be aligned with Accenture’s Life Sciences R&D vertical, working in Pharmacovigilance Operations. You will support end-to-end drug safety surveillance activities, ensuring timely and accurate handling of adverse event case reports in compliance with global regulatory requirements.

This is a great opportunity for freshers and early-career professionals to build a strong foundation in drug safety and pharmacovigilance operations within a global professional services leader.


Key Responsibilities

  • Manage affiliate mailbox and reconcile reports as per process requirements.

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

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

  • Ensure compliance with client guidelines and global pharmacovigilance regulations.

  • Work as an individual contributor within a collaborative team environment.

  • Adapt to rotational shifts as per project/business needs.


What We’re Looking For

  • Qualifications: Bachelor of Pharmacy (B.Pharm) or Master of Pharmacy (M.Pharm).

  • Knowledge or internship experience in drug safety / pharmacovigilance preferred.

  • Strong attention to detail and ability to follow regulatory and client-specific processes.

  • Good communication and teamwork skills.

  • Ability to work in fast-paced, process-driven environments.


Why Join Accenture?

  • Be part of a global leader with expertise across 40+ industries.

  • Work with top biopharma clients, supporting drug safety and patient-centric healthcare.

  • Gain exposure to advanced technology platforms and global regulatory compliance.

  • Continuous learning, certifications, and career development opportunities.

  • Inclusive workplace that values diversity, well-being, and innovation.


Equal Employment Opportunity:
Accenture is an equal opportunity employer, committed to providing a workplace free from bias where all individuals are respected, valued, and empowered.