Clinical Research Coordinator
3 days ago
Your Opportunity:
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**:Clinical Trials Unit, Cancer Care Alberta
- **Primary Location**:Cross Cancer Institute
- **Location Details**:As Per Location
- **Multi-Site**:Not Applicable
- **FTE**:1.00
- **Posting End Date**:17-NOV-2025
- **Temporary Employee Class**:Temp F/T Benefits
- **Date Available**:08-DEC-2025
- **Temporary End Date**:02-OCT-2026
- **Hours per Shift**:7.75
- **Length of Shift in weeks**:2
- **Shifts per cycle**:10
- **Shift Pattern**:Days
- **Days Off**:Saturday/Sunday
- **Minimum Salary**:$32.34
- **Maximum Salary**:$41.21
- **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**:
**Preferred Qualifications**:
Preference given to those with a bachelor’s level degree (health-related). Completion of an approved Clinical Research or Data Management Certificate Program. SoCRA or ACRP certification/membership. Familiar with using and creating spreadsheets, and various databases (e.g. InForm, RAVE) or electronic medical records (e.g. Netcare, ConnectCare, ARIA).
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