Olabisi Kesinro

Detail-oriented Clinical Research Assistant with 2+ years supporting regulated, protocol-driven research studies, including hands-on laboratory coursework from a BSc in Biochemistry. Skilled in specimen and sample documentation, chain-of-custody and temperature-log recordkeeping, source document and consent preparation, and data entry across multiple EDC systems (REDCap, SORMAS, ODK). ICH-GCP certified with completed training in TDG and IATA regulations for dangerous-goods/specimen shipment. Proven ability to follow step-by-step protocols precisely, identify and escalate discrepancies, and maintain accurate, audit-ready logs and filing systems in fast-paced, multi-study environments. Comfortable performing repetitive, accuracy-sensitive tasks and eager to grow into a lab-focused Clinical Research Coordinator role.

• Saisie de données
• Filing
• Google Workspace

1. Food Service Representative

   Trillium Health Partners

   oct. 2025 to Aujourd’hui

   • Collaborate daily with multidisciplinary healthcare professionals and care teams in a fast-paced acute-care hospital, strengthening communication and teamwork skills that transfer directly to a structured, multi-study clinical research environment. • Maintain accurate documentation and comply with hospital quality-assurance, OHSA, WHMIS, and HACCP standards, reflecting comfort with regulated, procedure-driven recordkeeping. • Manage multiple time-sensitive responsibilities while maintaining accuracy, professionalism, and confidentiality in a patient-centred setting.

2. Safety Officer

   Lateef Akanni Hussein Institute for Radiation Monitoring and Protection

   févr. 2023 to janv. 2025

   • Conducted compliance inspections and internal reviews to verify adherence to institutional policies, regulatory requirements, and quality standards. • Maintained controlled documentation and logs to support audit readiness and regulatory inspections, mirroring the accuracy required for temperature logs, handling logs, and shipment records. • Prepared compliance reports, monitored corrective actions, and communicated findings clearly to internal stakeholders.

3. Program Coordinator – Clinical Public Health Projects

   Nigeria CDC Emergency Operations Centre

   janv. 2020 to mai 2022

   • Operated within established research protocols to coordinate participant recruitment, screening, and consenting, and enrollment tracking across multi-site public health studies, liaising with investigators and Ethics Board (REB) staff on ethical and regulatory compliance. • Created, modified, and maintained source documents, informed consents, and information letters, applying Good Documentation Practice to keep Trial Master File and Investigator's Site File materials inspection- and audit-ready. • Completed accurate data entry and case report completion in multiple EDC systems (SORMAS, ODK), performing validation, reconciliation, and quality control to protect data integrity. • Tracked supplies, enrollment logs, and study timelines across multiple field sites; identified and escalated discrepancies rather than proceeding without clarification. • Delivered protocol and regulatory training to 50+ healthcare workers and field personnel; supported monitoring visits, quality-assurance reviews, and audit preparation.

4. Administrative Assistant

   Ministry of Health

   nov. 2015 to oct. 2016

   • Organized, maintained, and archived regulatory documentation using structured filing and labelling systems, supporting document management and version control. • Coordinated correspondence, approvals, and submissions while maintaining confidentiality, accuracy, and timely retrieval of records.

1. Humber Polytechnic

   Graduate Certificate, Clinical Research

2. University of Ibadan

   Master of Science, Public Health Biotechnology

   2017 to 2019

3. Crawford University

   Bachelor of Science, Biochemistry

   2011 to 2015

   laboratory-based coursework

• ICH-GCP Certification

  CITI Program

• Health Canada Division 5: Drugs for Clinical Trials Involving Human Subjects

  CITI Program

• Transportation of Dangerous Goods (TDG) and IATA

  CITI Program

• Ethical Conduct for Research Involving Humans

  TCPS 2: CORE-2022

• Responsible Conduct of Research (RCR)

  CITI Program

• Workplace Violence and Harassment Awareness

  Workplace Safety & Prevention Services

• Cultural Competency Skills in Clinical Research

  N2 Canada