Open to opportunities

Toyin Olusi

@toyinolusi

Message

Results-driven Senior Clinical Research Associate with project management expertise.

United Kingdom

Message

What I'm looking for

I am seeking a role that leverages my project coordination and regulatory expertise in clinical research.

I am a results-driven Senior Clinical Research Associate with four years of experience managing clinical trials from planning through close-out across various phases of oncology studies. My proven track record in project execution, site performance optimization, risk mitigation, and stakeholder management has equipped me with the skills necessary to drive compliance with ICH-GCP, MHRA, FDA, and EMA guidelines while ensuring quality deliverables across functional teams.

Throughout my career, I have demonstrated strength in leading interdisciplinary project teams, vendor oversight, and client communications. My role as a Clinical Site Manager at Roche involved managing over 20 site and field staff, ensuring regulatory compliance, and maintaining trial documents for audit-readiness. I am adept at coordinating efforts across clinical operations, data management, safety, and regulatory affairs to meet study goals, and I take pride in mentoring and training new Clinical Research Associates to foster knowledge transfer within the study team.

Experience

Work history, roles, and key accomplishments

Current

Clinical Site Manager / Senior CRA

Current

Roche via IQVIA UK

Jan 2025 - Present (8 months)

Led cross-functional study execution, managing 20+ site and field staff across phases including start-up, execution, and monitoring. Oversaw site readiness, documentation management, and project timelines to ensure regulatory and sponsor compliance.

Project Management Regulatory Compliance Documentation Management Vendor Management Stakeholder Management

Senior Clinical Research Associate

BeiGene via IQVIA UK

Dec 2023 - Jan 2025 (1 year 1 month)

Functioned as primary point of contact between sponsor and investigative sites; managed communication, training, and monitoring. Oversaw site progress including monitoring visits, SAE reporting, CRF completion, and risk-based data reviews.

Site management Regulatory Submissions Protocol Amendments Investigator Brochures

Clinical Research Associate I/II

IQVIA UK

Jun 2021 - Nov 2023 (2 years 5 months)

Managed all phases of clinical monitoring (initiation, interim, close-out), ensuring adherence to regulatory and sponsor standards. Reviewed site logs, safety documents, investigational product accountability, and patient informed consent records.

Education

Degrees, certifications, and relevant coursework

University of Northampton

Master of Science, Child and Adolescent Mental Health

Completed a Master of Science degree in Child and Adolescent Mental Health. This program provided advanced knowledge in mental health assessment, intervention, and support for young people.

Olabisi Onabanjo University

Bachelor of Science, Microbiology

Earned a Bachelor of Science degree in Microbiology. The curriculum covered fundamental principles of microbial biology, genetics, and their practical applications.