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Pharmacovigilance Services Associate

0-2 years
Not Disclosed
10 July 3, 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 – Accenture, Bengaluru (0–2 Years)

Job Summary:
Accenture is hiring for a Pharmacovigilance Services Associate in Bengaluru to support its Life Sciences R&D vertical. This entry-level opportunity is perfect for candidates with up to 2 years of experience in drug safety, ICSR case processing, and MedDRA coding. You will manage safety reports, ensure regulatory compliance, and contribute to improving patient safety for top global biopharma clients.


Key Responsibilities:

  • Manage affiliate mailbox and reconcile reports as per established SOPs

  • Perform data entry, MedDRA coding, and case processing for ICSRs

  • Execute follow-up communications for both serious and non-serious cases

  • Ensure timely and compliant submissions to regulatory authorities

  • Support safety database operations in line with client and regulatory standards

  • Maintain case documentation and quality standards throughout the reporting process

  • Collaborate with team members and follow detailed instructions to resolve routine tasks

  • Work under supervision and contribute to team goals as an individual contributor

  • May be required to work in rotational shifts based on project needs


Required Skills & Qualifications:

  • Bachelor's or Master’s degree in Pharmacy (BPharm/MPharm)

  • 0–2 years of experience in pharmacovigilance or drug safety operations

  • Understanding of ICSR processing and global regulatory reporting guidelines

  • Familiarity with safety databases and MedDRA coding

  • Strong attention to detail and data accuracy

  • Ability to follow processes and comply with regulatory standards

  • Good communication and adaptability in a team environment

  • Problem-solving skills and agility for quick learning

  • Willingness to work in a shift-based work environment if needed


Perks & Benefits:

  • Competitive salary with variable pay

  • Paid time off and structured work hours

  • Healthcare and wellness benefits

  • Global exposure in the life sciences domain

  • Training and certification opportunities

  • Inclusive work culture recognized as one of the World’s Best Workplaces™


Company Description:

Accenture is a global leader in professional services and healthcare innovation. With cutting-edge capabilities in digital, operations, and life sciences R&D, it supports leading biopharma clients across clinical trials, regulatory, and drug safety processes.


Work Mode: On-site (Bengaluru)
Experience Level: 0–2 years
Job Type: Full-time
Compensation Range: Not disclosed
Shift Requirements: Rotational shifts may apply


Call to Action:

Launch your career in pharmacovigilance with Accenture’s world-class Life Sciences team. Apply now to make a real impact in global drug safety and patient care.