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Pharmacovigilance Services New Associate

Accenture
Accenture
0-2 years
Not Disclosed
Bengaluru, India
10 March 12, 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

Company: Accenture
Location: Bengaluru, India
Job Type: Full-Time
Job ID: AIOC-S01630790
Industry: Life Sciences / Pharmacovigilance / Drug Safety

Experience Required: 0–2 Years
Education: MSc / Bachelor of Pharmacy (B.Pharm) / Master of Pharmacy (M.Pharm)

About Accenture
Accenture is a leading global professional services company specializing in digital transformation, cloud computing, and cybersecurity solutions. With a workforce of more than 784,000 professionals serving clients across 120+ countries, Accenture delivers services in Strategy and Consulting, Technology, Operations, and Accenture Song.

Within the Life Sciences sector, Accenture provides end-to-end support across the pharmaceutical value chain, including clinical research support, regulatory services, pharmacovigilance operations, and patient service solutions. The organization works with global biopharmaceutical companies to improve patient outcomes by combining scientific expertise, advanced technology, and data-driven insights.

Job Overview
Accenture is hiring a Pharmacovigilance Services New Associate to join its Life Sciences R&D team in Bengaluru. This entry-level pharmacovigilance role focuses on drug safety monitoring, adverse event case processing, and pharmacovigilance data management.

The selected candidate will support pharmacovigilance operations by managing safety cases, performing medical coding, and ensuring regulatory compliance for Individual Case Safety Reports (ICSRs). This role is ideal for life sciences graduates seeking to begin a career in pharmacovigilance, drug safety surveillance, and pharmaceutical regulatory compliance.

Key Responsibilities

  • Perform case identification and accurate data entry for Individual Case Safety Reports (ICSRs) in pharmacovigilance safety databases.

  • Conduct MedDRA coding for adverse events and medical information.

  • Support case processing, case validation, and submission activities in accordance with global pharmacovigilance regulations and client guidelines.

  • Manage follow-ups for safety cases and maintain accurate safety documentation.

  • Monitor and analyze drug safety information to identify potential adverse drug reactions.

  • Ensure adherence to pharmacovigilance standard operating procedures (SOPs) and regulatory compliance requirements.

  • Collaborate with internal pharmacovigilance teams to maintain data quality and reporting accuracy.

Required Skills and Competencies

  • Basic understanding of pharmacovigilance and drug safety surveillance processes.

  • Knowledge of adverse event reporting and ICSR processing.

  • Familiarity with MedDRA terminology and safety databases is preferred.

  • Strong attention to detail and data accuracy.

  • Good analytical and problem-solving abilities.

  • Effective written and verbal communication skills.

  • Ability to work in a structured, process-driven environment.

Roles and Responsibilities

  • Handle routine pharmacovigilance tasks using established guidelines and standard procedures.

  • Work closely with the immediate team and report to the direct supervisor for task management and guidance.

  • Execute assigned activities following detailed instructions and quality standards.

  • Contribute as an individual team member within a defined scope of work.

  • Ensure timely completion of tasks while maintaining compliance with internal quality and regulatory requirements.

  • Be flexible to work in rotational shifts based on project and client requirements.

Why Join This Role
This position offers an excellent opportunity for early-career professionals to gain hands-on experience in pharmacovigilance operations, drug safety reporting, and global regulatory compliance. Working with Accenture’s Life Sciences team provides exposure to international pharmacovigilance practices and the opportunity to build a strong foundation in pharmaceutical safety monitoring.

Job Location
Bengaluru, India.