- 10+ years of leadership experience in Drug Safety/Pharmacovigilance operations
- Leading a team of 50-200 people consisting of drug safety physicians and experts
- Hands-on experience of Business Development in Europe and US
- Well-networked with International Community of Pharma Experts
- Client engagement/Collaboration and overall stakeholder management
Core competency in set up and management of end to end Pharmacovigilance Unit of International standards ensuring delivery of:
- Aggregate report writing (PADER, PSUR, and Annual Safety Reports) and medical assessment
- Medical Monitoring
- Signal detection, analysis and evaluation
- Product Risk Management (REMS)
- PV systems validation
- Provide drug safety leadership and ensure thorough understanding of adverse event management, workflow elements and compliance with local regulatory guidelines and Global Product Safety (GPS) policies, procedures and processes.
- Maintain proficiency in current knowledge of all applicable regulatory guidelines and regulations relating to safety reporting
- Interact with clients and internal staff to provide advice and guidance on safety review issues; provide training and consultation to clients
- Assist Business Development for client development presentations that involve safety reporting as a potential service; provide adequate input into client proposals
- Identify training needs in Pharmacovigilance and work with Training Group to implement appropriate training
- Advise management on adequate budget and resource planning
- Well versed with operational multitude of safety databases i.e. ARGUS, ARISg, AERS, PVNet
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