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Pharmacovigilance Services New Associate

Accenture
0-1 years
INR 4 LPA – 5.5 LPA
Bangalore, India
1 June 18, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: HCPCS Level II, ICD-10-CM, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICD-10-PCS, ICH guidelines

Pharmacovigilance Services New Associate

Company: Accenture
Location: Bengaluru, India
Employment Type: Full Time
Experience Required: 0–1 Year
Qualification: Bachelor of Pharmacy (B.Pharm)


Job Overview

The Pharmacovigilance Services New Associate will support drug safety and pharmacovigilance activities within Accenture's Life Sciences R&D practice. The role involves case processing, adverse event management, MedDRA coding, safety data review, and compliance with global pharmacovigilance regulations.

This is an entry-level opportunity for pharmacy graduates interested in building a career in Pharmacovigilance, Drug Safety, and Regulatory Operations.


Key Responsibilities

Case Processing & Safety Data Management

  • Create and manage Individual Case Safety Reports (ICSRs).

  • Perform case identification and data entry into safety databases.

  • Conduct MedDRA coding for adverse events and medical history.

  • Process safety cases according to client requirements and regulatory guidelines.

  • Review source documents and extract relevant safety information.

Pharmacovigilance Operations

  • Monitor adverse event reports received from various sources.

  • Support case follow-up activities and obtain missing information when required.

  • Ensure timely processing and submission of safety reports.

  • Maintain compliance with global pharmacovigilance requirements.

  • Support drug safety surveillance activities.

Regulatory Compliance

  • Follow applicable global regulatory requirements.

  • Ensure adherence to client SOPs and pharmacovigilance procedures.

  • Maintain accurate and complete case documentation.

  • Support audit readiness and quality compliance activities.

Data Quality & Documentation

  • Verify accuracy and completeness of safety data.

  • Perform quality checks on processed cases.

  • Maintain documentation in accordance with regulatory standards.

  • Ensure timely completion of assigned deliverables.

Team Collaboration

  • Work closely with supervisors and team members.

  • Participate in process training and knowledge-sharing activities.

  • Support operational goals and quality objectives.

  • Follow established workflows and process guidelines.


Qualifications

Education

  • Bachelor of Pharmacy (B.Pharm)

Preferred Educational Background

  • Pharmacy

  • Life Sciences

  • Medical Sciences

  • Biotechnology

  • Related Healthcare Disciplines


Experience

  • 0–1 year of experience.

  • Freshers are eligible to apply.

  • Internship or training exposure in Pharmacovigilance is an advantage.