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📍 Location: [Not mentioned – you may add if available]
🏢 Company: Accenture
🧪 Department: Life Sciences – Pharmacovigilance & Drug Safety Surveillance
📅 Experience Required: 1 to 3 Years
🎓 Qualifications: Bachelor or Master of Pharmacy (B.Pharm/M.Pharm)
🧾 About Accenture
Accenture is a global professional services company with capabilities in digital, cloud, security, consulting, technology, operations, and AI-driven insights. With 699,000+ employees across 120 countries, we help clients create real impact and drive innovation at scale.
🔗 Visit: www.accenture.com
🧬 About the Role
You will join the Pharmacovigilance Operations team under the Life Sciences R&D vertical. This division supports biopharma clients in managing clinical trials, regulatory documentation, drug safety operations, and patient experience.
🧪 Key Responsibilities
- Manage affiliate mailbox and reconcile reports as per internal SOPs
- Perform written follow-ups for both serious and non-serious cases
- Process ICSRs including:
- Case identification
- Data entry
- MedDRA coding
- Case submission & follow-up
- Ensure compliance with global regulatory guidelines and client-specific protocols
🔍 What We’re Looking For
- Strong knowledge of pharmacovigilance & drug safety surveillance
- Experience in drug safety data entry and case management
- Familiarity with MedDRA coding and regulatory submission standards
- Good communication skills and willingness to work in rotational shifts
👤 Work Style & Scope
- Solve routine problems using general SOPs and team guidance
- Interact primarily with your direct team and supervisor
- Perform as an individual contributor on a focused scope of work
- Receive detailed instructions for new assignments and moderate instructions for daily tasks
🔄 Shift: Rotational (as required)
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