Oladapo Oladumiye

Coordinated end-to-end oncology and metabolic patient care workflows across multidisciplinary clinical teams. Served as a primary clinical liaison handling documentation, scheduling, and authorization, maintaining audit-ready HIPAA-compliant EMR records.

Coordinated Phase I-IV clinical trial site activities supporting principal investigators from initiation through close-out. Managed patient screening and enrollment, informed consent verification, Veeva EDC data queries, investigational product accountability, AE/SAE reporting, and audit readiness.

Translated complex scientific, technical, and regulatory workflows into structured SOPs and governance documentation. Managed multiple concurrent remote deliverables independently using strong self-direction and time management.

Coordinated full lifecycle Phase I-IV oncology and multi-therapeutic clinical trials from site initiation through close-out. Supported principal investigators with patient enrollment, source document review, CRF completion, pharmacovigilance escalation, investigational product accountability, and ICH-GCP/FDA-aligned regulatory documentation using multiple EDC systems.

Built and managed physician and healthcare provider accounts. Developed communication and relationship skills applicable to investigator relationship management and site engagement.

Earned an M.D. from Belarusian State Medical University (2016–2023) with clinical rotations in oncology, cardiology, endocrinology, hematology, neurology, internal medicine, and multi-therapeutic care.