Date Posted: 09/11/2026Req ID: 50127Faculty/Division: Temerty Faculty of MedicineDepartment: Department of Pharmacology and ToxicologyCampus: St. George Downtown TorontoPosition Number: 00060049 Existing Vacancy: Yes Description: About us:Home to over 40 departments and institutes, the University of Toronto's Temerty Faculty of Medicine lies at the heart of the Toronto Academic Health Science Network and is a global leader in ground-breaking research and education, spanning clinical medicine, basic science and the rehabilitation sciences sectors.Your opportunity: The Department of Pharmacology and Toxicology is among the oldest in North America. We offer training in pharmacology and toxicology to both undergraduate and graduate students who may subsequently go on to exciting research, regulatory and administrative careers in academic, industrial, and healthcare provision settings. We also provide training to professional programs such as Medicine and Pharmacy.As the Clinical Research Coordinator, you will assist with participant recruitment, consent, scheduling, and testing to determine study eligibility. Drawing on your strong organizational skills and attention to detail, you will ensure that data and biosamples are accurately collected, coded, and maintained in accordance with research ethics and institutional standards. Your ability to communicate effectively and provide supportive interactions with participants will contribute to the smooth and ethical execution of study activities.Your responsibilities will include: Delivering presentations and posting advertisements to recruit study participants Determining participant eligibility against study criteria, preparing consent forms and organizing study materials Scheduling and conducting participant assessments in English, Mandarin, or Cantonese while traveling to participant locations as required to conduct study visits or collect samples and materials Maintaining research databases and records, ensuring that all information is accurately coded, entered, and stored in compliance with confidentiality and research integrity standards Handling biosamples and assisting with the collection, labeling, and transport of biological materials in accordance with safety and research protocols Resolving issues that arise during test administration and escalating concerns to the Principal Investigator or senior research staff as required Essential Qualifications: Bachelor’s degree in a relevant discipline or acceptable combination of equivalent experience Minimum one 1 year of experience working with older adults in a research or clinical study setting Demonstrated experience conducting participant testing and assessments in accordance with research protocols and ethical standards Experience preparing consent forms using templates Demonstrated experience maintaining research databases and records including accurate data entry, coding of quantitative research data, and generating reports Experience taki
