Job
Description
As a Pharmacovigilance Services Specialist at Accenture, your role involves performing Medical Assessment activities related to drug safety Pharmacovigilance for the Individual Case Safety Reports. You will be responsible for various tasks including: - Performing Medical Review of ICSRs according to the client SOPs/Manuals - Prioritizing cases based on Regulatory clock date and seriousness criteria, ensuring timely completion as per client SOP - Reviewing all applicable Medical Review Fields for accuracy - Planning, organizing, and managing daily work to meet service level timelines and deliverables - Reviewing MedDRA coding of reported terms in Cases, suggesting additional events as needed - Conducting causality assessment of serious cases and relevant non-serious cases with Company Remarks when applicable - Performing labelling of events in applicable cases - Providing Medical Expertise to the case processing team as required - Offering training/mentoring to team members when necessary In addition, you will be involved in creating and managing case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for ICSRs in the safety database following client guidelines and global regulatory requirements. Qualifications required for this role include: - MBBS/MD degree - 3 to 5 years of experience - Proficiency in English (International) Accenture is a global professional services company known for its expertise in digital, cloud, and security services across various industries. With a team of 699,000 professionals operating in more than 120 countries, Accenture focuses on delivering value through technology and human ingenuity. To learn more, visit www.accenture.com. As a Pharmacovigilance Services Specialist at Accenture, your role involves performing Medical Assessment activities related to drug safety Pharmacovigilance for the Individual Case Safety Reports. You will be responsible for various tasks including: - Performing Medical Review of ICSRs according to the client SOPs/Manuals - Prioritizing cases based on Regulatory clock date and seriousness criteria, ensuring timely completion as per client SOP - Reviewing all applicable Medical Review Fields for accuracy - Planning, organizing, and managing daily work to meet service level timelines and deliverables - Reviewing MedDRA coding of reported terms in Cases, suggesting additional events as needed - Conducting causality assessment of serious cases and relevant non-serious cases with Company Remarks when applicable - Performing labelling of events in applicable cases - Providing Medical Expertise to the case processing team as required - Offering training/mentoring to team members when necessary In addition, you will be involved in creating and managing case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for ICSRs in the safety database following client guidelines and global regulatory requirements. Qualifications required for this role include: - MBBS/MD degree - 3 to 5 years of experience - Proficiency in English (International) Accenture is a global professional services company known for its expertise in digital, cloud, and security services across various industries. With a team of 699,000 professionals operating in more than 120 countries, Accenture focuses on delivering value through technology and human ingenuity. To learn more, visit www.accenture.com.
