Full Time

Pharmacovigilance Services Manager

Accenture
Bengaluru
Salary Not Disclosed
Posted 10/03/2026

About the Role

Why This Role Matters

Pharmacovigilance professionals play a crucial role in ensuring the safety and effectiveness of medicines. By monitoring adverse drug reactions, evaluating safety data, and ensuring regulatory compliance, Pharmacovigilance Services Managers help protect patient health while supporting pharmaceutical companies in maintaining global safety standards.

Job Description

Accenture is hiring a Pharmacovigilance Services Manager in Bengaluru, Karnataka. This role focuses on medical review, adverse event assessment, and drug safety surveillance while managing pharmacovigilance operations in compliance with global regulatory requirements. The position involves working closely with internal teams and clients to ensure accurate case processing and safety monitoring of pharmaceutical products.

Key Features of the Role

• Position: Pharmacovigilance Services Manager
• Company: Accenture
• Location: Bengaluru, Karnataka, India
• Industry: IT Services / Healthcare Consulting / Pharmacovigilance
• Employment Type: Full-Time (On-site)
• Experience Required: 7–11 Years

Responsibilities

• Conduct medical review and assessment of adverse events for seriousness, causality, and labeling
• Ensure pharmacovigilance processes comply with global regulatory requirements and client SOPs
• Monitor and analyze safety data related to pharmaceutical products
• Manage case identification, data entry, MedDRA coding, and case processing for Individual Case Safety Reports (ICSRs)
• Ensure timely submission and follow-up of pharmacovigilance cases in safety databases
• Identify and assess complex safety issues related to medications
• Provide solutions and recommendations based on safety data analysis
• Collaborate with internal teams and client stakeholders on pharmacovigilance operations
• Manage medium to large teams or pharmacovigilance workstreams
• Follow strategic direction from senior management while achieving operational goals

Required Qualification

• MBBS or MD degree

Important Requirements

• 7–11 years of experience in pharmacovigilance or drug safety surveillance
• Strong analytical and problem-solving abilities
• Knowledge of pharmacovigilance processes and global regulatory guidelines
• Excellent written and verbal communication skills
• Ability to work collaboratively with cross-functional teams
• Willingness to work in rotational shifts if required

What We Offer

• Opportunity to work with a global professional services organization
• Exposure to international pharmacovigilance and regulatory practices
• Collaboration with multinational clients and healthcare organizations
• Professional growth within a large global network

Experience and Skills

• Pharmacovigilance and drug safety surveillance
• Adverse event evaluation and safety data analysis
• Risk management and regulatory compliance
• MedDRA coding and ICSR processing
• Strong analytical thinking and decision-making skills
• Team management and collaboration abilities

Company Overview

Accenture is a global professional services company specializing in digital, cloud, and security solutions. With more than 784,000 employees serving clients in over 120 countries, Accenture provides services in strategy, consulting, technology, and operations. The company supports organizations across multiple industries, including healthcare and life sciences, with advanced technology and intelligent operations solutions.

FAQs

  1. What qualifications are required for this role?
    Candidates must hold an MBBS or MD degree.

  2. How much experience is required?
    The role requires 7 to 11 years of experience in pharmacovigilance or drug safety.

  3. Where is the job located?
    The position is based in Bengaluru, Karnataka, India.

  4. Is shift work required?
    Yes, the role may require working in rotational shifts.

Application Tips

• Highlight your experience in pharmacovigilance and drug safety monitoring
• Mention expertise in MedDRA coding and ICSR processing
• Emphasize analytical and risk management skills
• Include experience managing teams or pharmacovigilance projects

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