Open to opportunities

Oladapo Oladumiye

@oladapooladumiye1

Message

Physician-trained Clinical Research Coordinator with 5+ years managing Phase I-IV trials.

United States

Message

What I'm looking for

I’m looking for a Clinical Research Coordinator role where I can own site-level execution end-to-end, strengthen ICH-GCP compliance and audit readiness, and collaborate closely with PI teams, sponsors, and CROs to improve patient enrollment and data quality.

I’m a physician-trained (M.D.) Clinical Research Coordinator with 5+ years of Phase I-IV clinical trial coordination experience across oncology, neurology, cardiovascular-adjacent, metabolic, infectious disease, and pediatric therapeutic areas. I support principal investigators and manage site-level study activities from initiation through close-out—patient screening and enrollment, informed consent, regulatory documentation, investigational product accountability, AE/SAE reporting, and EDC management.

My work is grounded in ICH-GCP / FDA / IRB compliance and audit readiness. I’m experienced in source document review (SDR), CRF completion and EDC query resolution, protocol deviation management, and pharmacovigilance workflows, including timely reporting of adverse events and serious adverse events to sponsors and IRBs.

Across roles, I’ve strengthened cross-functional stakeholder coordination and improved execution in high-volume environments. Most notably, I improved patient enrollment timelines by 20% by redesigning screening and scheduling workflows and aligning stakeholders—while maintaining audit-ready, HIPAA-compliant documentation. Recently, I’ve applied site management and patient coordination skills as a PET/CT Coordinator, reinforcing my clinical workflow expertise for research populations.

Experience

Work history, roles, and key accomplishments

Current

PET/CT Coordinator

Current

RadNet

Apr 2026 - Present (3 months)

Coordinated end-to-end oncology and metabolic patient care workflows in a high-volume outpatient setting, serving as a primary clinical liaison for documentation, scheduling, and authorization. Maintains audit-ready, HIPAA-compliant EMR documentation and validates imaging indications against diagnostic protocols.

Clinical Liaison Documentation Resolution Imaging Indication Validation Oncology Care Metabolic Disease Coordination

Clinical Research Coordinator

Sanmora Bespoke Clinical Research Solutions

Mar 2025 - Apr 2026 (1 year 1 month)

Coordinated site-level activities across Phase I-IV clinical trials in oncology, neurology, infectious disease, COPD, and metabolic therapeutic areas, supporting principal investigators from initiation through close-out. Managed screening/enrollment, informed consent compliance, source document review, Veeva EDC verification and query resolution, investigational product accountability, ISFs, audit

Phase I IV Clinical Trial Coordination Veeva Investigational Product Accountability Audit Readiness Pharmacovigilance ICH GCP FDA IRB Compliance SOP And ICF Documentation

Freelance Consultant

Centific

Aug 2023 - Aug 2024 (1 year)

Translated complex scientific, technical, and regulatory workflows into structured SOPs and governance documentation to support regulatory-writing needs. Managed multiple concurrent remote deliverables independently with strong time management.

Scientific Documentation Technical Documentation Governance Regulatory Writing Independent Remote Deliverable Management Time Management

Clinical Research Coordinator

Minsk City Hospital No. 10

Jun 2020 - Jun 2023 (3 years)

Coordinated the full lifecycle of Phase I-IV oncology and multi-therapeutic clinical trials from site initiation through close-out, managing site-level activities including patient enrollment, source document review, CRF completion, investigational product accountability, and regulatory documentation. Supported principal investigators, administered IV infusions/injections for HBV and pediatric ane

Phase I IV Clinical Trial Coordination Patient Enrollment CRF Investigational Product Accountability ICFs Subject Safety Data Verification Pharmacovigilance Escalation IV Infusions And Injections Administration (HBV Pediatric Anemia Trials)Veeva Florence ICH GCP FDA Compliance

Medical Sales Representative

Vonadi

Jun 2019 - May 2020 (11 months)

Built and managed physician and healthcare provider accounts, strengthening communication and relationship-building skills relevant to site engagement. Developed interpersonal skills applicable to investigator relationship management.

Communication Stakeholder Engagement Sales & Account Management

Education

Degrees, certifications, and relevant coursework

Belarusian State Medical University

Doctor of Medicine (M.D.), Medicine

2016 - 2023

Grade: Summa cum laude

Earned a Doctor of Medicine (M.D.) degree with clinical rotations spanning oncology, cardiology, endocrinology, hematology, neurology, internal medicine, and multi-therapeutic care. Graduated summa cum laude.