Provide in-depth medical/scientific expertise in the safety evaluation and risk management of key GSK assets
Ensure scientifically sound review and interpretation of data and management of safety issues
Make recommendations for the further characterization, management, and communication of safety risks
Support the pharmacovigilance and benefit-risk management of the assigned portfolio of GSK global assets
Accountable for the product team level GSK asset Benefit Risk profile and Benefit Risk management
Requirements
Health Sciences/Health Care Professional degree required (e.g., BSc, MS, PhD, RN/BSN/MSN, NP, RPh/B Pharm/Pharm D)
Significant pharmacovigilance experience relating to Safety Evaluation and Risk Management, encompassing both clinical development and post-marketing activities
Knowledge/experience of international pharmacovigilance requirements (e.g., ICH, GVP modules, CIOMS initiatives) and drug development and approval processes
Experience working in large matrix organizations
Benefits
health care and other insurance benefits (for employee and family)