Pharmacovigilance Services Associate

Roles & Responsibilities
• Perform end-to-end pharmacovigilance operations including case identification, intake, and processing of ICSRs
• Enter, review, and manage safety data in pharmacovigilance databases as per client SOPs and global regulations
• Perform MedDRA coding, case processing, submissions, and follow-ups within defined timelines
• Ensure compliance with global regulatory requirements and client-specific guidelines
• Support drug safety surveillance activities including adverse event detection and evaluation
• Analyze safety data collected from clinical trials, healthcare providers, and patients
• Work as an individual contributor within a defined scope under team and supervisor guidance
• Solve routine operational issues using standard procedures and established guidelines
• Participate in rotational shifts as per business requirements

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

Experience
• 1 to 3 years of experience in Pharmacovigilance / Drug Safety Operations

Skills
• Strong knowledge of pharmacovigilance and drug safety processes
• Hands-on experience with ICSR processing and safety databases
• Familiarity with MedDRA coding and regulatory guidelines (ICH, FDA, EMA)
• Good attention to detail and documentation skills
• Ability to work effectively within a team environment
• Basic problem-solving and analytical skills

About the Organization
Accenture is a global professional services company with expertise in digital, cloud, and security, serving clients across more than 40 industries. Through its Life Sciences R&D vertical, Accenture supports leading biopharma companies with clinical, pharmacovigilance, and regulatory solutions that improve patient outcomes worldwide.