Pharmacovigilance Services New Associate (Drug Safety Associate Entry Level)

Accenture; Bengaluru; On-site; INR 350,000 - 550,000; Full time

Job summary

Accenture in Bengaluru, India, invites applications for a Pharmacovigilance Services New Associate (Drug Safety Associate Entry Level). This entry-level role focuses on drug safety data handling, ICSR processing, and regulatory compliance within Life Sciences R&D.

Ideal candidates have MSc Life Sciences or B.Pharm/M Pharm, with exposure to pharmacovigilance concepts, MedDRA coding, and a keen eye for detail. Freshers are welcome; rotational shifts may apply as per business needs.

Qualifications

• MSc (Life Sciences) / B.Pharm / M.Pharm or equivalent.
• Strong understanding of pharmacovigilance and drug safety.
• Basic knowledge of MedDRA coding and ICSR lifecycle preferred.
• Good analytical skills and attention to detail.
• Effective communication and teamwork abilities.

Responsibilities

• Identify, enter, and process IC S Rs (ICSRs).
• Perform MedDRA coding and ensure safe data entry.
• Manage case workflows including follow-ups, submissions, lifecycle tracking.
• Monitor ADRs and support signal detection activities.
• Ensure compliance with global pharmacovigilance regulations and client guidelines.
• Collaborate with internal teams for quality review and case closure.
• Maintain data accuracy, completeness, and regulatory timelines.
• Support routine pharmacovigilance operations under supervision.

Skills

Analytical skills

Communication skills

Teamwork

Education

MSc Life Sciences

Bachelor of Pharmacy

Master of Pharmacy

Tools

MedDRA coding

ICSR processing

Job description

Pharmacovigilance Services New Associate (Drug Safety Associate Entry Level) Location: Bengaluru, India

Company: Accenture

Job ID: AIOC-Shidden_mobile6

Job Type: Full-Time

Experience Required: 02 Years (Freshers Eligible)

About the Company

Accenture is a leading global professional services organization specializing in digital, cloud, and security solutions. With operations in over 120 countries and a workforce of more than 700,000 professionals, Accenture delivers cutting-edge services across Strategy, Consulting, Technology, and Operations. Within Life Sciences, the organization plays a pivotal role in enabling pharmaceutical and biotechnology companies to accelerate innovation, ensure patient safety, and meet global regulatory standards.

Job Overview

This entry-level Pharmacovigilance role is part of Accentures Life Sciences R&D division, focusing on drug safety and risk management. The position is ideal for freshers and early-career professionals looking to build a strong foundation in Pharmacovigilance Operations, including Individual Case Safety Report (ICSR) processing and safety data management.

Key Responsibilities

• Perform case identification, data entry, and processing of Individual Case Safety Reports (ICSRs)
• Conduct MedDRA coding and ensure accurate safety database entry
• Manage case workflows including follow-ups, submissions, and lifecycle tracking
• Monitor adverse drug reactions (ADRs) and support signal detection activities
• Ensure compliance with global pharmacovigilance regulations and client-specific guidelines
• Collaborate with internal teams for quality review and case closure
• Maintain data accuracy, completeness, and regulatory timelines in safety reporting
• Support routine pharmacovigilance operations under supervision

Required Qualifications

• MSc (Life Sciences) / Bachelor of Pharmacy / Master of Pharmacy
• Strong understanding or academic exposure to Pharmacovigilance and Drug Safety
• Basic knowledge of MedDRA coding and ICSR lifecycle preferred
• Good analytical skills and attention to detail
• Effective communication and teamwork abilities

Desired Skills and Competencies

• Understanding of Pharmacovigilance Operations and regulatory frameworks
• Familiarity with clinical research and drug safety processes
• Ability to work in a structured, process-driven environment
• Willingness to work in rotational shifts as per business requirements

Work Environment and Role Scope

• Entry-level individual contributor role with defined responsibilities
• Tasks are guided by standard operating procedures and supervision
• Opportunity to gain hands-on experience in global pharmacovigilance projects
• Exposure to real-world drug safety case processing and regulatory workflows

Why This Role is Important for Your Career

This position serves as a gateway into the Pharmacovigilance and Drug Safety domain. It provides foundational experience in ICSR processing, regulatory compliance, and safety data handling, making it an ideal starting point for careers such as Drug Safety Associate, Medical Reviewer, or Pharmacovigilance Specialist.

Equal Employment Opportunity Statement

Accenture is committed to creating an inclusive workplace. All employment decisions are based on merit, qualifications, and business needs, without discrimination based on race, gender, age, disability, religion, sexual orientation, or any other protected status.