Description:As a Clinical Research Coordinator, you will provide support for research studies through the identification, collection, and reporting of clinical trial data. You will compile research, reports and regulatory documents as required by the protocol, and study/sponsor. This involves ensuring research information is timely, accurate, valid, meaningful, and to the sponsor's satisfaction, and that studies are run according to local and global regulations.
- Transition Company: Cancer Care Alberta
- Classification: Clinical Resrch Coord (ACB)
- Union: HSAA Facility PROF/TECH
- Unit and Program: Owerko Center for Clinical Trials
- Primary Location: Arthur Child Cancer Centre
- Location Details: As Per Location
- Multi-Site: Not Applicable
- FTE: 1.00
- Posting End Date: 02-JUL-2026
- Temporary Employee Class: Temp F/T Benefits
- Date Available: 13-JUL-2026
- Temporary End Date: 16-JUL-2027
- Hours per Shift: 7.75
- Length of Shift in weeks: 2
- Shifts per cycle: 10
- Shift Pattern: Days
- Days Off: Saturday/Sunday
- Minimum Salary: $35.34
- Maximum Salary: $45.03
- Vehicle Requirement: Not Applicable
Required Qualifications: Completion of a minimum two year diploma or certificate in a health care related field. Minimum of two years' clinical research experience.
Additional Required Qualifications: Previous experience in coordinating complex clinical trials. Prior experience working with pharmaceutical sponsors and CROs. Strong negotiation, multitasking and communication skills. Adaptable and able to coordinate and manage numerous simultaneous projects and meet strict deadlines. Knowledge of oncology medical terminology. ICH-GCP training and familiarity with clinical trial regulatory reporting requirements. Excellent computer skills and experience working with Microsoft Office programs. Able to work well in a team environment and able to complete individual assigned projects or tasks according to strict deadlines.
Preferred Qualifications: Clinical Trial experience (preferably in oncology or complex interventional trials). Society of Clinical Research Associates (SoCRA) or ACRP certification/membership. Oncology experience. Experience in study start up, Research Ethics Board and Health Canada applications, experience using clinical trial (electronic case report form) eCRF software, various databases or electronic medical records (e.g. Connect Care, Netcare). Knowledge of clinical trial regulatory framework.
