Pharmacovigilance Services Assoc Manager
Designation: Pharmacovigilance Services Assoc Manager
Qualifications:MBBS/MD
Years of Experience:3 to 14 years
Language - Ability:English(Domestic) - Expert
About Accenture
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What would you do? Responsible for medical review of the aggregate and RMP report within agreed timeframes and to a high standard of accuracy, in compliance with client’s standard operating procedures and global regulatory requirements. Pharmacovigilance Services involve the detection, assessment, and prevention of adverse effects related to pharmaceutical products. These services ensure the safety and efficacy of medications by monitoring and analyzing data from clinical trials, healthcare providers, and patients. The goal is to identify potential risks and take appropriate actions to protect patient health. They also help pharmaceutical companies comply with regulatory requirements. Effective pharmacovigilance services are essential for maintaining public trust in medications. Manage and develop individual case narratives describing adverse events for inclusion in regulatory submissions and safety reports for completed/interim clinical study reports.
What are we looking for? Responsible for medical review of the aggregate and RMP report within agreed timeframes and to a high standard of accuracy, in compliance with client’s standard operating procedures and global regulatory requirements. Medical review experience in AR, RMP and signal management
Roles and Responsibilities: • Participate in KOM, project planning/strategy making meeting. • Ensuring the aggregate reports and RMP documents are medically relevant, complete, consistent and accurate. • Providing inputs/insights from review of aggregated and RMP data aligned to client’s processes(s) and SOPs. • Addresses all previous Health authority comments and adhoc requests received from Health authority. • Review and provide any noteworthy cases & published studies including pregnancy registries. • Discuss and provide medical analysis for all relevant sections of AR and RMP • To provide the conclusion regarding the current safety profile of the product. • Address all medical queries/comments raised by the Client. • Perform QC of all the assigned aggregate reports and RMP documents. • Complete all trainings, assigned by internally or client on respective LMS within due date. • Responsible for knowledge sharing, coaching, review and providing feedback of reports medically analyzed by the mentees. • Notify critical and major deviations (referred, as Quality Issues) within one business days, and minor deviations within three business days to Accenture Quality Management team. Ensure to meet all SLAs and KPIs. • Incorporate comments from Client (or external) stakeholders into the draft RMP/ associated documents and seek clarification where applicable.
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