Research I
Role Overview
The Clinical Research Coordinator works with the Alberta Health Services Clinical Research Unit at the Arthur J.E. Child Comprehensive Cancer Centre in Calgary.
The role supports clinical trials and cancer research in collaboration with research teams and internal and external stakeholders.
Key Skills for This Role
Full Job Posting
Role overview
The Clinical Research Coordinator works with the Alberta Health Services Clinical Research Unit at the Arthur J.E. Child Comprehensive Cancer Centre in Calgary.
The role supports clinical trials and cancer research in collaboration with research teams and internal and external stakeholders.
Responsibilities
- Support assigned studies and research projects, ensuring information is timely, valid, and meaningful.
- Identify, collect, review, and report clinical trial data and study information.
- Prepare and submit research and regulatory documents required by study protocols and sponsors.
- Monitor study compliance and facilitate clinical trial processes according to protocol.
- Assist with participant recruitment and initiate study or trial consent.
- Work with research nurses, investigators, department staff, sponsors, CROs, and other research team members.
- Complete laboratory work to support research activities when needed.
Required qualifications
- Diploma or degree in a health- or science-related field; professional registration where required.
- At least 2 years of clinical research experience, including experience coordinating complex clinical trials.
- Prior experience working with pharmaceutical sponsors and CROs.
- Strong negotiation, multitasking, communication, and organizational skills; ability to meet strict deadlines.
- Knowledge of oncology medical terminology, ICH-GCP training, and clinical trial regulatory reporting requirements.
- Excellent computer skills and experience with Microsoft Office.
- Ability to work independently and as part of a team, using judgment, initiative, and discretion.
Preferred qualifications
- Clinical trial experience, preferably in oncology or complex interventional trials; oncology experience.
- SoCRA or ACRP certification or membership.
- Experience with study start-up, Research Ethics Board and Health Canada applications, eCRF software, databases, or electronic medical records.
- Knowledge of the clinical trial regulatory framework.
Schedule and employment
- Regular full-time position, 1.00 FTE, with day shifts.
- Shifts are 7.75 hours, 10 shifts per two-week cycle; regular days off are Saturday and Sunday.
Compensation
- Posted minimum salary is $38.80 and maximum salary is $51.16; the description does not state a pay period.
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