Emmanuel Anteyi MD, MS, FRCP
Clinician Medical Monitor, VRD, Clinical Research and Development @ Pfizer
About
Experienced clinical research leader with a proven track record in advancing innovative therapies through strategic trial design, execution, and cross‑functional collaboration. Skilled at translating complex data into actionable insights that drive regulatory success and patient impact. I bring expertise in clinical development strategy, evidence generation, and medical leadership, with a focus on aligning science and strategy to address unmet medical needs. Passionate about patient‑centered outcomes, I thrive in guiding programs from concept to real‑world impact while ensuring compliance and scientific rigor. Currently pursuing leadership opportunities where I can contribute to meaningful innovation and accelerate therapies that improve lives.
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United States
Pharmaceuticals
Cross-functional Collaborations, Electronic Data Capture (EDC), Safety reviews and trends, Clinical Efficacy endpoints review, Medical Education, Clinical Research Management Systems, Data Analysis, Clinical Monitoring, Clinical Protocol, Patient Safety, Drug Development, Team Leadership, Clinical Development, Regulatory Submissions, Data Review, Clinical Supervision, Oncology, Budgeting, Presentations, Risk Management
Experience

Clinical Research Medical Monitor
Silver Spring, MD
• Routine and Directed Post-Approval Compliance medical monitoring of WRAIR sponsored /collaborative research including minimal risk (MR), Greater than minimal risk (GTMR) and ,FDA-regulated clinical trials in diverse therapeutic areas of Immunology, Vaccines, Cardiometabolic, Infectious and emerging viral diseases, genomics, hematology, Devices and sleep disorders

Medical Director/Medical Monitor,Clinical Development
Newtown Square, Pennsylvania, PA 19073, United States
•Clinical Trial Team Lead provides Medical Monitoring, clinical trial management and operations of KT301 Phase 2b and KT 302 Phase 2 clinical trials of biotherapeutic products in Nephrology cardiometabolic and immunology therapeutic areas at 26 sites in USA and Asia. •Direct medical monitoring to ensure protocol compliance, adherence to subject selection criteria, prompt safety reports, data integrity and quality, carrying out root-cause analysis and prompt CAPA management for clinical trials at 26 sites located in USA and Asia. Reviews, determined and provides clarifications on protocol, ICF, IB from clinical trial sites and regulatory agencies (IRB and FDA). •External Assessor, University of Delaware Collaborative Graduate Research on Microbial Genomics and Metabolomics in chronic kidney disease. Contributed to NIH/ SBIR funding submissions for Biotherapeutics and Genomic research grants. Published over 5 research papers in peer review journals on Inflammation, Clinical trial protocol, cardiometabolic and renal syndromes.

Attending Chief Physician-Internal Medicine / Professor/Clinical Research , Dept of Medicine
Abuja, Nigeria
Attending Chief Internal Medicine Physician and Clinical Lead Internal Medicine/Nephrology clinics. Regional Coordinator, Graduate Research & Medical Residency Training programs in Internal Medicine. •Clinical Team Lead, Patient safety and Pharmacovigilance committee, Hospital Drug Formulary, and Medical Devices committee. Provided Patient safety expertise for approved pharmaceutical products across Nephrology, cardio-metabolic, Infectious Diseases and hematology pharmaceutical products •Clinical investigator and site leader for Phases 1-3 multicenter collaborative and industry sponsored clinical research •Program Director, Physicians Collaborative Training and Research of The Royal College of Physicians (UK) and West African College of Physicians. •Adj Professor, Dept of Internal Medicine,Bingham College of Medicine, at Jos Campus and .Assistant Professor, Dept of Internal Medicine, College of Medicine, University of Jos
Emmanuel Anteyi MD, MS, FRCP's Contact Information
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