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Pharmacovigilance Services New Associate

Accenture
Accenture
0-2 years
Not Disclosed
Bengaluru, Karnataka, India
10 Feb. 17, 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

Pharmacovigilance Services New Associate (Drug Safety Associate)
Location: Bengaluru, Karnataka, India
Job Type: Full-Time
Experience Level: 0–2 Years
Job No.: AIOC-S01628146
Company: Accenture

Job Overview

Accenture is hiring a Pharmacovigilance Services New Associate to join its Life Sciences R&D vertical in Bengaluru. This entry-level pharmacovigilance role is ideal for pharmacy and life sciences graduates seeking to build a career in drug safety, regulatory compliance, and global pharmacovigilance operations.

The selected candidate will support pharmacovigilance and drug safety surveillance activities for leading biopharmaceutical clients, ensuring compliance with global regulatory requirements and maintaining high standards of patient safety.

Experience Required

  • 0 to 2 years of experience in pharmacovigilance, drug safety, or clinical research (freshers eligible)

  • Strong understanding of pharmacovigilance principles and ICSR processing preferred

  • Knowledge of MedDRA coding and safety databases is an advantage

Educational Qualifications

  • MSc (Life Sciences or related field)

  • Bachelor of Pharmacy (B.Pharm)

  • Master of Pharmacy (M.Pharm)

Key Responsibilities

  • Perform case identification, data entry, and processing of Individual Case Safety Reports (ICSRs)

  • Conduct MedDRA coding and ensure accurate documentation in safety databases

  • Manage case follow-ups and submissions in compliance with global pharmacovigilance regulations

  • Support drug safety surveillance activities including adverse event data review and analysis

  • Adhere to client-specific guidelines and international regulatory standards

  • Escalate complex issues to supervisors as per standard operating procedures

  • Maintain data quality, accuracy, and compliance across all assigned tasks

Role Expectations

  • Solve routine pharmacovigilance and drug safety tasks based on predefined guidelines

  • Work closely with team members and direct supervisors

  • Follow structured instructions for daily case processing activities

  • Operate as an individual contributor within a defined scope of responsibilities

  • Willingness to work in rotational shifts, if required

Core Competencies

  • Basic understanding of global pharmacovigilance regulations

  • Knowledge of adverse event reporting and drug safety monitoring

  • Attention to detail and data accuracy

  • Strong analytical and documentation skills

  • Ability to work in a process-driven, compliance-focused environment

About Accenture

Accenture is a global professional services organization with leading capabilities in digital, cloud, and security. With operations in over 120 countries and a workforce of more than 784,000 professionals, Accenture delivers Strategy and Consulting, Technology, and Operations services across more than 40 industries.

Within Life Sciences R&D, Accenture supports pharmaceutical and biopharmaceutical companies across clinical development, regulatory affairs, pharmacovigilance, and patient services. The organization helps life sciences companies accelerate innovation while maintaining strict regulatory compliance and patient-centric outcomes.

Why Apply for This Pharmacovigilance Role?

  • Entry-level opportunity in pharmacovigilance and drug safety operations

  • Exposure to global biopharma clients and international regulatory standards

  • Structured training and professional development environment

  • Career pathway in clinical safety, regulatory affairs, and life sciences operations

This Pharmacovigilance Services New Associate position in Bengaluru is ideal for pharmacy and life sciences graduates looking to start a career in drug safety, adverse event reporting, and regulatory compliance within a global pharmaceutical services environment.

Apply now through The Pharma Daily to explore entry-level pharmacovigilance jobs in India and advance your career in drug safety and life sciences.