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Role & Responsibilities
• Perform case intake and processing of Individual Case Safety Reports (ICSRs)
• Handle Adverse Event (AE) and Serious Adverse Event (SAE) data
• Code medical terms using MedDRA and WHO-DD
• Perform quality checks on safety case data
• Support global drug safety and compliance activities
• Work on post-marketing surveillance and COVID-related safety data
• Ensure adherence to ICH-GCP, GVP, and regulatory timelines
Qualifications & Experience
• B.Pharm, M.Pharm, BSc / MSc Life Sciences
• Freshers with internship or project exposure in Pharmacovigilance, Clinical Research, Drug Safety, or COVID safety projects
Skills
• Basic understanding of pharmacovigilance concepts
• Good communication and documentation skills
• Willingness to work in rotational shifts
About the Company
• Accenture supports global pharmaceutical clients through structured pharmacovigilance and drug safety operations, offering corporate exposure and stable career growth