Job Title: Pharmacovigilance Services Associate (Drug Safety & ICSR Processing)
Location: Bengaluru
Job Type: Full-Time
Experience Required: 0–2 Years (1–3 Years Preferred)
Industry: Pharmacovigilance / Drug Safety / Life Sciences
About the Company
Accenture is a leading global professional services organization with expertise in digital, cloud, and security. With operations in over 120 countries, Accenture delivers innovative solutions across Strategy, Consulting, Technology, and Operations, supporting life sciences organizations in advancing healthcare outcomes and patient safety.
Job Overview
The Pharmacovigilance Services Associate will be part of the Life Sciences R&D vertical, supporting pharmacovigilance and drug safety operations. This role focuses on monitoring, assessing, and reporting adverse events to ensure compliance with global regulatory standards and to safeguard patient health. It is an excellent opportunity for early-career professionals to build expertise in drug safety and regulatory compliance.
Key Responsibilities
Perform case identification, data entry, and processing of Individual Case Safety Reports (ICSRs)
Conduct MedDRA coding and ensure accurate classification of adverse events
Manage case follow-ups, submissions, and lifecycle activities within safety databases
Ensure compliance with global pharmacovigilance regulations and client-specific guidelines
Support detection, assessment, and reporting of adverse drug reactions
Maintain high-quality documentation and data accuracy in safety systems
Collaborate with internal teams to meet operational timelines and quality standards
Handle routine tasks with defined guidelines and escalate complex issues when required
Eligibility Criteria
Bachelor’s or Master’s degree in Life Sciences, including BSc, B.Pharm, or M.Pharm
0–2 years of experience in pharmacovigilance or drug safety (1–3 years preferred)
Required Skills and Competencies
Basic understanding of pharmacovigilance and drug safety processes
Knowledge of ICSR processing and MedDRA coding
Familiarity with global regulatory requirements and compliance standards
Strong attention to detail and data accuracy
Good analytical and problem-solving skills
Effective communication and teamwork abilities
Willingness to work in rotational shifts
Compensation and Benefits
Competitive salary and performance-based incentives
Opportunity to work with global pharmaceutical clients
Structured training and career development programs
Exposure to end-to-end pharmacovigilance operations
Collaborative and inclusive work environment
Why Join Accenture
Work with a global leader in life sciences and healthcare consulting
Gain hands-on experience in pharmacovigilance and regulatory services
Opportunity to contribute to improving patient safety worldwide
Strong focus on learning, innovation, and career growth
Equal Opportunity Employer
Accenture is committed to creating an inclusive and diverse workplace. All qualified applicants will be considered for employment without discrimination based on any protected characteristics.
This role is ideal for fresh graduates and early-career professionals looking to start or advance their career in pharmacovigilance, drug safety, and regulatory affairs within a global organization.
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