Kingsley Urakpo

WORK HISTORY

EDUCATION

SKILLS

ABOUT KINGSLEY URAKPO

I am a Consultant Pharmaceutical Physician, UK PMST-certified in Pharmaceutical Medicine (Faculty of Pharmaceutical Medicine, Royal College of Physicians), with extensive experience across clinical development, pharmacovigilance/drug safety, medical affairs, and regulatory strategy, supporting biopharmaceutical companies from early development through late-stage and post-marketing.I have worked across biotech, CROs, and global pharmaceutical organisations, advising on drug discovery, Phases I–IV clinical development, safety governance, and commercialization readiness. My work bridges clinical science and business strategy, enabling sponsors to make risk-informed, regulator-ready decisions across the product lifecycle.Core areas of expertise include:• Clinical Development Strategy (Phases I–IV)• Pharmacovigilance & Drug Safety (signal detection, RMP/REMS, DSUR, PBRER)• Medical Affairs & Medical Monitoring• Regulatory Affairs & Health Authority interactions (FDA, EMA, MHRA, Health Canada, PMDA, TGA)• Clinical & Safety Due Diligence for asset evaluation and transactionsI have supported programs across oncology, cardiometabolic disease, respiratory, rheumatology, dermatology, gastroenterology, neurosciences, and rare diseases, collaborating with cross-functional teams to accelerate development timelines while maintaining patient safety and regulatory compliance.In addition to advisory and leadership roles, I am the Founder and Managing Member of NADDBio, where I provide strategic consulting and execution support to biopharma sponsors seeking experienced physician leadership without permanent overhead.I work with biopharma companies, investors, and CROs seeking senior clinical and safety expertise on a consulting, fractional, or project basis.