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Pharmacovigilance Services Associate

0-2 years
Not Disclosed
10 July 24, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science 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, Karnataka, India
Experience Required: 0–2 years
Job Type: Full-time
Compensation: Not disclosed
Job ID: AIOC-S01593592


Job Summary

Accenture is seeking a Pharmacovigilance Services Associate to join its Life Sciences R&D vertical in Bengaluru. This role involves drug safety surveillance, MedDRA coding, case processing, ICSR submission, and managing pharmacovigilance operations to ensure compliance with global regulations. Freshers or candidates with up to 2 years of experience in drug safety or pharmacovigilance operations are encouraged to apply.


Key Responsibilities

  • Manage affiliate mailboxes, case identification, and data entry for ICSRs.

  • Perform MedDRA coding, follow-up activities, and case processing as per client guidelines.

  • Ensure compliance with global pharmacovigilance regulations and safety database standards.

  • Support the creation and submission of safety reports for both serious and non-serious cases.

  • Collaborate with team members and supervisors to ensure accurate case handling.

  • Work in rotational shifts as required.


Required Skills & Qualifications

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

  • 0–2 years of experience in pharmacovigilance, drug safety, or clinical data review.

  • Strong understanding of MedDRA, ICSR processing, and pharmacovigilance operations.

  • Basic knowledge of GVP and ICH guidelines.

  • Good communication and problem-solving skills.

  • Ability to work with safety databases and PV documentation.


Perks & Benefits

  • Opportunity to work with a global leader in life sciences operations.

  • Structured training programs in drug safety and regulatory compliance.

  • Access to certifications and learning modules for skill development.

  • Comprehensive well-being support including mental, physical, and financial wellness programs.

  • Inclusive and diverse work culture.


Company Description

Accenture is a global leader in digital, cloud, and security solutions, offering strategy, consulting, technology, and operations services across 40+ industries. With over 775,000 professionals worldwide, Accenture’s Life Sciences R&D vertical focuses on pharmacovigilance, clinical trials, and regulatory services to help biopharma companies bring therapies to market efficiently.


Work Mode

On-site – Bengaluru, Karnataka (rotational shifts).


Call to Action

If you are passionate about drug safety and pharmacovigilance, apply today for the Pharmacovigilance Services Associate role at Accenture. Submit your application online now!