Job Title: Pharmacovigilance Services Analyst
Job ID: AIOC-S01620520
Location: Chennai, Tamil Nadu, India
Job Type: Full-Time
Experience Required: 2–5 Years
Industry: Pharmacovigilance | Drug Safety | Life Sciences
Accenture is a global professional services organization with leading capabilities in digital, cloud, and security. With deep expertise across more than 40 industries, Accenture delivers Strategy & Consulting, Technology, Operations, and Accenture Song services through the world’s largest network of Advanced Technology and Intelligent Operations centers. Serving clients in over 120 countries, Accenture helps life sciences organizations drive innovation, compliance, and patient-centric outcomes.
Accenture is hiring a Pharmacovigilance Services Analyst to support global drug safety and pharmacovigilance operations within its Life Sciences R&D vertical. This role focuses on Individual Case Safety Report (ICSR) processing, safety surveillance, and regulatory compliance, supporting leading biopharmaceutical companies in maintaining patient safety and meeting global regulatory requirements.
Perform end-to-end ICSR case processing, including case identification, data entry, MedDRA coding, medical review support, submissions, and follow-ups
Ensure case processing activities comply with client SOPs and global pharmacovigilance regulations
Manage safety cases within validated safety databases as per defined timelines
Support adverse event detection, assessment, and documentation from multiple data sources
Maintain high-quality documentation and data accuracy in all pharmacovigilance activities
Analyze and resolve low to medium complexity pharmacovigilance issues
Collaborate with internal team members and supervisors to meet quality and productivity targets
Support operations that may require working in rotational shifts
2–5 years of hands-on experience in Pharmacovigilance / Drug Safety Operations
Strong knowledge of ICSR processing, MedDRA coding, and safety database workflows
Understanding of global pharmacovigilance regulations and reporting timelines
Ability to work effectively in a team-oriented, process-driven environment
Strong attention to detail and analytical skills
Japanese Language Ability (Elementary Level)
JLPT certification N3 to N5 preferred
Any Graduate, B.Pharm, or M.Pharm with relevant pharmacovigilance experience
Individual contributor role with defined scope of work
Moderate supervision with detailed guidance for new assignments
Limited client interaction; primary collaboration with internal stakeholders
Opportunity to work with global life sciences and biopharma clients
Exposure to international pharmacovigilance processes and safety systems
Strong learning, upskilling, and career growth opportunities
SEO & GPT-Optimized Keywords:
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