Pharmacovigilance Services New Associate

About the Role 
Join Accenture’s Life Sciences R&D team to support global drug safety operations. You will process Individual Case Safety Reports (ICSRs) and ensure compliance with international pharmacovigilance regulations. This role is ideal for freshers and early-career professionals entering pharmacovigilance and drug safety.

Key Responsibilities
Process ICSRs including case intake, data entry, MedDRA coding, submissions and follow-ups
Maintain data accuracy, timelines and audit readiness
Ensure compliance with SOPs and global regulatory requirements
Support routine pharmacovigilance surveillance activities

Eligibility Criteria
Educational Qualification
Bachelor of Pharmacy (B.Pharm) or Bachelor’s degree in Life Sciences

Experience
0 to 1 year of experience (Freshers eligible)

Skills Required
Basic understanding of pharmacovigilance and drug safety concepts
Good attention to detail and data accuracy
Ability to follow SOPs and regulatory timelines
Basic knowledge of MedDRA coding preferred
Good communication and documentation skills
Willingness to work in a process-driven, compliance-focused environment