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Job Description & How to Apply Below
The Clinical Research Coordinator will be based at the Colon Cancer Screening Centre (CCSC), Cal Wenzel Precision Health Building, University of Calgary, Foothills Campus. This position reports to the CCSC Director Research.
The Clinical Research Coordinator will be responsible for the organization and conduct of a clinical research study, including recruitment of participants, scheduling participant activities, data collection and data entry.
Summary of
Key Responsibilities
Coordinate and administer a clinical research project per established study protocol and procedure manuals
Coordinate participant recruitment across multiple clinics, care pathways, and recruitment strategies
Conduct consent discussions and obtain informed consent from participants
Contact participants, schedule research activities, conducting telephone and in clinic interviews and ensuring data is submitted accurately
Interview participants, enter data, and administer questionnaires
Provide guidance to participants regarding clinical sample collection
Assist in the collection, delivery, entry, verification, management, analysis and reporting of data
Responsible for maintaining ethical and confidentiality standards
Ensure relevant research methodology is applied, and proper handling of all research material is used
Build and sustain collaborative relationships with specialists and healthcare teams to support study enrolment goals
Travel to local study sites to collect, transport, and manage biospecimens in accordance with study protocols and regulatory requirements
Design, develop, and maintain study materials, including participant-facing documents, recruitment materials, and study protocols
Mentor, train, and support junior research staff, students, and trainees in study procedures, participant interactions, and data management practices
Qualifications / Requirements
Bachelors Degree in a relevant health related field (required)
Masters Degree (preferred)
5 years of relevant clinical research experience (clinical trials, multicenter studies, registry studies) is preferred
Recognized research professional certification (e.g. CCRP, Certified Clinical Research Professional) an asset
Experience working with the public is a strong asset
Experience working in a post-secondary institution or hospital is an asset
Knowledge of health and scientific terminology is a strong asset
Proficiency in Microsoft Office Programs
Experience using REDCAP is a strong asset
Excellent organization skills and attention to detail
Knowledge of Good Clinical Practice (GCP) and the Tri-Council Policy Statement:
Ethical Conduct for Research Involving Humans (TCPS2) is required
Self-motivated and demonstrated ability to function independently and within a team environment are required
Knowledge of surgical pathways is an asset
Prior experience in a clinical or research environment in preferred, with demonstrated familiarity working in patient-facing or academic health settings
Final date to receive applications
September 1, 2026
We would like to thank all applicants in advance for submitting their resumes. Please note, only those candidates chosen to continue on through the selection process will be contacted.
This position is part of the AUPE bargaining unit, and falls under the Specialist/Advisor Job Family, Phase 2.
For a listing of all management and staff opportunities at the University of Calgary, view our Management and Staff Careers website.
About The University Of Calgary
UCalgary is Canada's entrepreneurial university, located in Canada's most enterprising city. It is a top research university and one of the highest-ranked universities of its age. Founded in 1966, its 36,000 students experience an innovative learning environment, made rich by research, hands‑on experiences and entrepreneurial thinking. It is Canada's leader in the creation of start‑ups. Start something today at the University of Calgary.
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