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Victoria Olanrewaju

@victoriaolanrewaju

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I’m a Principal Clinical Research Associate and manager delivering compliant Phase I–IV trials with CRO leadership.

United States

Message

What I'm looking for

I’m seeking a leadership role in global clinical operations where I can oversee CROs, strengthen site performance, and ensure compliant Phase I–IV trials with strong inspection-ready documentation.

I’m a Certified Clinical Research Associate (CCRP – SOCRA) with nursing training and 7+ years of progressive experience leading global Phase I–IV clinical trials. I bring patient centered judgment to research operations while staying focused on compliant, high-quality execution.

In my current role as Global Clinical Operations Principal CRA / Manager, I oversee multiple CROs across U.S. and European regions to ensure high quality monitoring and regulatory compliance. I develop monitoring plans, CRFs, study tools, and CRO training materials, and I lead contract negotiations, budget reviews, and vendor qualification activities. I also manage study start up, site qualification, and regulatory submissions including FDA 510k and device filings, while reviewing and approving CRA reports and supporting inspection readiness.

Previously as a Senior Clinical Research Associate / Site Manager – IDS Specimen Management, I conducted monitoring for Phase I–IV oncology and pharma trials, strengthening data quality and patient safety. I contributed to YODA BD MiniDraw system clearance, oversaw capillary finger stick device studies, and led feasibility assessments, site selection, SIVs, continuous monitoring, retraining, and site closeout. I also created CRFs, reviewed protocols and ICFs, and helped develop monitoring plans.

I’ve also supported clinical operations through biospecimen logistics, TMF reconciliation, and query/data cleaning, ensuring documentation quality and audit readiness. Across roles, I’ve built a reputation for improving study timelines, strengthening site performance, and collaborating closely with R&D, Regulatory, Quality, and Clinical Operations teams to deliver reliable outcomes.

Experience

Work history, roles, and key accomplishments

Current

Nursing Graduate Clinical Rotations

Current

St. Luke's University Health Network

Mar 2026 - Present (4 months)

Provided patient-centered care on a medical-surgical unit under RN supervision during clinical rotations. Performed patient assessments and vital signs, supported mobility and fall prevention, and followed infection control, wound care, IV therapy, and post-operative monitoring procedures.

patient assessment Vital Signs Monitoring Mobility Support Patient Education Interdisciplinary Communication Infection Control Wound Care IV Therapy Post Operative Monitoring

Current

Global Clinical Ops Principal CRA/Manager

Current

Becton Dickinson (BD)

Sep 2024 - Present (1 year 10 months)

Oversee CROs across U.S. and European regions to ensure high-quality monitoring and regulatory compliance. Develop monitoring plans and study tools, lead vendor qualification and contract/budget reviews, and support inspection readiness including device filings and FDA 510(k) submissions.

CRO Oversight Vendor Management CRA Report Review Study Start Up Regulatory Submissions 510(K)Device Filings Inspection Readiness Clindex Oracle Microsoft Office

Senior Clinical Research Associate/Site

Becton Dickinson (BD)

Sep 2021 - Jan 2024 (2 years 4 months)

Conducted monitoring for Phase I–IV oncology and pharma trials, focusing on data quality and patient safety. Supported device-related work (YODA BD MiniDraw System) and led feasibility, site/investigator qualification, site monitoring activities, and study milestone closeout.

Data Quality Patient Safety Capillary Finger Stick Device Studies feasibility studies Site Selection Monitoring Close Out Recruitment support

Clinical Research Associate - Specimen

Becton Dickinson (BD)

Jul 2020 - Sep 2021 (1 year 2 months)

Supported query resolution, data cleaning, and TMF documentation, and assisted with site selection, initiation, monitoring, and closeout. Trained site staff on protocol procedures and biospecimen handling while coordinating biospecimen logistics and vendor activities.

Query Resolution Data Cleaning TMF Site Selection Site Initiation Site Monitoring Close Out Vendor coordination Biospecimens

Biospecimen Specialist

Celgene Pharmaceuticals

Nov 2019 - Mar 2020 (4 months)

Managed biospecimen logistics for oncology trials, including tracking, reconciliation, and shipment coordination. Coordinated sample collection kits with manufacturing and distribution partners and reviewed biomarker-related documents for accuracy and compliance.

Trackings Reconciliations Logistics Coordination Analytical Lab Vendor Collaboration Biomarker Document Review (ICFs Protocols

Clinical Application Specialist III / CRA

Siemens Healthineers

Sep 2018 - Apr 2019 (7 months)

Monitored hematology and HIV trials using Atellica diagnostic instruments. Conducted site visits to support regulatory compliance and data quality, and provided training to site staff while supporting protocol adherence and CRF review.

Clinical Trial Monitoring Atellica Diagnostic Instruments HIV Trials Regulatory Compliance Data Quality CRFs Review GCP Compliance

TMF Specialist

Prolong Pharmaceuticals

Jul 2018 - Sep 2018 (2 months)

Led TMF reconciliation and study closeout for a sickle cell clinical trial. Ensured audit readiness and compliance with SOPs and ICH GCP by resolving documentation gaps and finalizing archiving.

Audit Readiness Documentation Gap Resolution E Archiving