Pharmacovigilance Services New Associate

Roles & Responsibilities
• Create and manage case identification and data entry for Individual Case Safety Reports (ICSRs)
• Perform MedDRA coding, case processing, submission, and follow-ups in the safety database
• Ensure compliance with client guidelines and global regulatory requirements
• Monitor and assess safety data related to pharmaceutical products
• Detect, evaluate, and document adverse events and drug-related problems
• Collect and analyze safety data from clinical trials, healthcare professionals, and patients
• Resolve routine issues by following established guidelines and standard procedures
• Work closely with team members and supervisors for task completion
• Adhere strictly to SOPs and regulatory compliance standards
• Support pharmacovigilance and regulatory activities within Life Sciences R&D vertical
• Work in rotational shifts as required

Qualification
• MSc
• Bachelor of Pharmacy (B.Pharm)
• Master of Pharmacy (M.Pharm)

Experience
• 0 to 1 year of experience in pharmacovigilance or drug safety (Freshers can apply)

Skills
• Basic understanding of Pharmacovigilance and Drug Safety Surveillance
• Knowledge of ICSR processing and MedDRA coding
• Good analytical and problem-solving skills
• Strong attention to detail
• Ability to follow detailed instructions and work under supervision
• Good communication and teamwork skills
• Willingness to work in rotational shifts

About the Company
Accenture is a global professional services company offering services in Strategy, Consulting, Technology, and Operations. With a strong presence in Life Sciences R&D, Accenture supports leading biopharma companies in clinical research, regulatory services, and pharmacovigilance to improve patient outcomes worldwide.