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Pharmacovigilance Services Associate

Accenture
Accenture
1-3 years
preferred by company
10 Jan. 13, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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 ID: AIOC-S01622134
Employment Type: Full-Time
Experience Required: 1–3 Years
Location: Bengaluru, India
Functional Area: Pharmacovigilance Operations / Drug Safety
Industry: Life Sciences & Clinical Research


Job Overview

We are hiring a Pharmacovigilance Services Associate to support global drug safety and pharmacovigilance operations within a life sciences R&D environment. This role is ideal for pharmacy graduates with hands-on exposure to ICSR processing, safety database operations, and regulatory compliance, looking to grow their career in global pharmacovigilance services.

The position focuses on case intake, data entry, medical coding, case processing, submissions, and follow-ups, ensuring adherence to client-specific SOPs and international regulatory requirements.


About the Organization

Accenture is a global professional services leader with capabilities across digital, cloud, security, technology, and operations. With a presence in over 120 countries and a workforce of more than 784,000 professionals, Accenture partners with leading biopharmaceutical and healthcare organizations to deliver end-to-end solutions across clinical research, pharmacovigilance, regulatory services, and patient safety.


Key Responsibilities

Pharmacovigilance & Drug Safety Operations

  • Perform end-to-end ICSR processing, including case identification, triage, data entry, and quality review in the global safety database.

  • Conduct MedDRA coding for adverse events and WHO-Drug coding for suspect and concomitant medications.

  • Process serious and non-serious cases in compliance with client SOPs, regulatory timelines, and global pharmacovigilance requirements.

  • Manage case submissions and follow-ups, ensuring accurate and timely reporting.

Case Management & Compliance

  • Review safety data from multiple sources, including clinical trials, healthcare professionals, and patient reports.

  • Ensure completeness, accuracy, and consistency of safety cases prior to submission.

  • Support ongoing pharmacovigilance surveillance activities to detect, assess, and prevent adverse drug reactions.

Team Collaboration & Operational Support

  • Work as an individual contributor within a structured team environment, following defined workflows and quality standards.

  • Interact primarily with immediate team members and direct supervisors.

  • Follow detailed instructions for daily operational tasks and moderate guidance for new assignments.

  • Participate in rotational shifts as per business requirements.


Education & Experience

Educational Qualifications:

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

Experience Requirements:

  • 1 to 3 years of experience in pharmacovigilance, drug safety, clinical research, or related life sciences roles.

  • Experience with ICSR processing and safety databases is highly desirable.


Required Skills & Competencies

  • Working knowledge of pharmacovigilance operations and drug safety surveillance.

  • Familiarity with global regulatory requirements for safety reporting.

  • Proficiency in medical terminology, MedDRA coding, and case narratives.

  • Basic to intermediate experience with safety databases and MS Office tools.

  • Strong attention to detail and ability to follow SOP-driven processes.

  • Good written and verbal English communication skills.

  • Ability to work independently within a defined scope and meet turnaround timelines.


Why Join This Role

  • Opportunity to work with leading global biopharmaceutical clients.

  • Exposure to international pharmacovigilance regulations and safety systems.

  • Structured career growth within clinical research and drug safety domains.

  • Continuous learning and skill development in a global delivery environment.


Apply Now

If you are a pharmacy graduate with experience in pharmacovigilance and drug safety operations and are looking to advance your career with global exposure, apply now through thepharmadaily.com.


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