Pharmacovigilance Services Senior Analyst

Role Overview Accenture is seeking an experienced Pharmacovigilance Senior Analyst to join its Life Sciences R&D vertical in Bengaluru. This role sits within the Pharmacovigilance and Regulatory sub-offering, where you will collaborate with some of the world's leading biopharmaceutical companies to strengthen drug safety surveillance frameworks and improve patient outcomes. Accenture operates across more than 120 countries, bringing together over 784,000 professionals with deep expertise spanning 40-plus industries, making it one of the most innovative environments in life sciences operations today. Key Responsibilities As a Senior Analyst in Pharmacovigilance Operations, you will manage end-to-end Individual Case Safety Report (ICSR) processing, which includes case identification, accurate data entry, MedDRA coding, case processing, regulatory submission, and timely follow-ups within the safety database. You will ensure all activities strictly adhere to client-specific guidelines and applicable global pharmacovigilance regulations. The role involves detecting, evaluating, and monitoring adverse drug reactions and other drug-related safety signals gathered from clinical trials, healthcare professionals, and patients. You will analyse increasingly complex drug safety scenarios, interact with internal peers and occasionally with client stakeholders, and contribute to maintaining the integrity and compliance of pharmacovigilance operations. Required Qualifications See requirements section below. Why Join Us At Accenture, you become part of a globally connected team that is redefining how life sciences companies operate at the intersection of science, technology, and human insight. You will work in an intellectually stimulating environment, gain exposure to international regulatory standards, and grow your expertise within a company that is consistently at the forefront of intelligent operations and digital health transformation.

Bachelor of Pharmacy (B.Pharma) or Master of Pharmacy (M.Pharma) from a recognised institution 5 to 8 years of hands-on experience in pharmacovigilance or drug safety operations Proficiency in ICSR case processing including data entry, MedDRA coding, and regulatory submissions Sound knowledge of global pharmacovigilance regulations and safety database management Experience monitoring and evaluating adverse drug reactions and drug-related safety signals Familiarity with clinical trials processes and life sciences R&D environment Strong analytical and problem-solving skills with the ability to handle complex safety cases independently Ability to work with minimal supervision on routine tasks and moderate guidance on new assignments Good interpersonal and communication skills for peer-level and client interactions Willingness to work in rotational shifts as required by the project

Opportunity to work with leading global biopharmaceutical companies Exposure to international pharmacovigilance and regulatory standards Career growth within Accenture's Life Sciences R&D vertical Access to Accenture's global network of Advanced Technology and Intelligent Operations centres Collaborative and innovation-driven work culture Full-time permanent employment with industry-standard compensation