Toronto, Ontario, Canada
I am a Clinical Research Coordinator with experience supporting Phase II–III clinical trials, bringing a strong foundation in data integrity, regulatory compliance, and patient-centred research delivery. With over 8 years of experience as a UK-registered paediatric and neonatal intensive care nurse, I offer a unique perspective that bridges frontline clinical care with high-quality research execution. My background in caring for critically ill infants and children, combined with my Master of Public Health (MPH), has strengthened my understanding of population health, evidence-based practice, and the broader impact of clinical research. This dual perspective enables me to contribute to studies that not only improve individual patient outcomes, but also drive meaningful, system-level change. Now based in Toronto, I am actively pursuing licensure with the College of Nurses of Ontario and seeking opportunities in clinical research where I can continue to contribute to impactful, patient-focused studies.
▪ Relocated from the UK to Toronto, establishing long-term residency in Ontario ▪ Spent several months travelling across Australia, Southeast Asia, and Japan, developing cultural awareness, adaptability, and global perspective ▪ Completed online CITI training certificates and in-person 'Career Readiness' training with ACCEP-IEHP to support transition into research-focused roles in Toronto
▪ Worked regular agency shifts whilst completing MPH and then alongside research roles ▪ Assessed and triaged patients, prioritising care and initiating appropriate acute interventions ▪ Maintained nursing competencies and clinical skills (wound care, neurological observations, medication administration, nebulisers/inhalers, IM injections etc.) with direct patient care ▪ Strong time-management skills developed working in a fast-paced, high-volume environment
▪ Coordinated 6 concurrent clinical trials sponsored by major pharmaceutical companies (Amgen, GSK, Novartis, Sanofi) ensuring adherence to protocol and regulatory requirements ▪ Facilitated participant screening and recruitment, and assisted with ethically informed consent, supporting timely study enrolment targets and participant retention ▪ Ensured timely resolution of data queries and accurate reporting and management of adverse events (AEs/SAEs), maintaining data integrity and participant safety
▪ Worked on real-life projects to gain experience writing for a medical communications agency ▪ Received positive feedback on my publication writing abilities and range of formatting approaches