Accenture has announced a new opportunity for experienced pharmacovigilance professionals through its latest Pharmacovigilance Services Associate recruitment in Bengaluru. This position is ideal for candidates with a Bachelor of Pharmacy (B.Pharm) or Master of Pharmacy (M.Pharm) degree and 1-3 years of experience in drug safety, ICSR processing, MedDRA coding, and pharmacovigilance operations.

The role offers an excellent opportunity to work with one of the world’s leading professional services organizations supporting global biopharmaceutical companies in pharmacovigilance and drug safety surveillance activities.

Job Overview

About Accenture

Accenture is a global professional services company specializing in digital transformation, cloud computing, artificial intelligence, consulting, and operations services. With over 790,000 employees serving clients in more than 120 countries, Accenture supports leading pharmaceutical and biotechnology companies through its Life Sciences Research & Development division.

The company’s pharmacovigilance and regulatory services help global healthcare organizations ensure patient safety, regulatory compliance, and efficient drug safety monitoring.

Key Responsibilities

The selected Pharmacovigilance Services Associate will be responsible for:

Case Processing Activities

• Perform case identification and intake of adverse event reports.
• Conduct accurate data entry into safety databases.
• Process Individual Case Safety Reports (ICSRs).
• Ensure compliance with global pharmacovigilance regulations.

MedDRA Coding

• Perform medical coding using MedDRA terminology.
• Ensure accuracy and consistency of coding activities.
• Review and validate coded medical information.

Drug Safety Surveillance

• Monitor adverse events and safety information.
• Support pharmacovigilance operations activities.
• Assist in signal detection and safety evaluation processes.

Regulatory Compliance

• Prepare and submit safety reports according to client requirements.
• Manage case follow-ups and reconciliation activities.
• Maintain adherence to regulatory guidelines and SOPs.

Documentation & Quality

• Ensure complete and accurate documentation.
• Support quality review processes.
• Maintain audit readiness and compliance standards.

Required Qualifications

Candidates must possess:

Educational Qualifications

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

Experience Requirements

• 1 to 3 years of pharmacovigilance experience.
• Prior experience in drug safety case processing preferred.
• Knowledge of ICSR workflow and safety databases.

Technical Skills

• Pharmacovigilance Operations
• Drug Safety Surveillance
• ICSR Processing
• MedDRA Coding
• Adverse Event Reporting
• Case Management
• Regulatory Compliance
• Safety Database Management

Preferred Skills

Candidates with the following competencies will have an advantage:

• Strong analytical abilities.
• Attention to detail.
• Good communication skills.
• Ability to work in a team environment.
• Time management skills.
• Knowledge of global pharmacovigilance regulations.
• Understanding of GVP guidelines.

Why Join Accenture?

Working at Accenture offers several benefits:

• Opportunity to work with leading global pharmaceutical clients.
• Exposure to international pharmacovigilance projects.
• Career growth in life sciences and drug safety.
• Learning and development programs.
• Diverse and inclusive work culture.
• Global exposure and networking opportunities.
• Competitive compensation and employee benefits.

Who Should Apply?

This role is suitable for:

• B.Pharm graduates with pharmacovigilance experience.
• M.Pharm professionals seeking drug safety careers.
• Drug Safety Associates looking for career advancement.
• Pharmacovigilance professionals with ICSR experience.
• Candidates experienced in MedDRA coding and case processing.

How to Apply

Application Link