Job Type






Clinical Research Coordinator - Clinical Trials Unit Edmonton

Alberta Health Services

Alberta Health Services Edmonton Canada

1 week ago

Your Opportunity:

Are you an experienced clinical trials professional looking for an interesting, challenging position? Do you enjoy working in a team environment on exciting projects involving new cutting-edge cancer therapies? If so, you may be the person we are looking for. This 9-month temporary Clinical Trials Coordinator position may be assigned to assist various teams/areas of the Unit. They report to CTU Management and are responsible for facilitating a variety of clinical trial processes and completing delegated study tasks. Responsibilities may include Prepare REB application submissions and progress reports, submit SAE's & IND safety reports and draft study consent forms. Complete and maintain regulatory forms and critical documents/binders for Clinical Trials. Developing systems to organize, plan and track workflow related to clinical trial activities to ensure timely documentation and data submissions. Abstract data to complete study forms, flow sheets, or CRF’s as... required by protocol. Review source documents and case report forms with site teams/study representatives and resolve data queries. Prepare and maintain study accrual statistics. Coordinate and prepare for monitoring visits, site audits, and regulatory inspections. Develop and maintain strong relationship(s) with PI’s, hospital personnel and representatives from outside agencies regarding ongoing conduct of clinical research. Register patients and inform appropriate personnel of assigned study treatment, notify team of communications regarding adverse drug reaction reports and ensure SAE safety documentation is completed.


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.

Classification: Clinical Resrch Coord (ACB) Union: HSAA Facility PROF/TECH Unit and Program: Clinical Trials Unit, Cancer Care Primary Location: Cross Cancer Institute Location Details: As Per Location Multi-Site: Not Applicable FTE: 1.00 Posting End Date: 26-MAY-2023 Temporary Employee Class: Temp F/T Benefits Date Available: 04-JUL-2023 Temporary End Date: 05-APR-2024 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:

Prior experience working with pharmaceutical sponsors and CRO’s. An ability to multi-task effectively in a busy area with multiple interruptions and competing demands. Strong communication skills. Adaptable and able to coordinate and manage numerous simultaneous tasks or projects while maintaining and meeting strict deadlines within a busy team environment. Experience working with Microsoft Office programs. Familiar with using and creating spreadsheets, and using various databases (e.g. InForm, RAVE). Experience with ethics submission systems (IRISS, REMO) and electronic medical records (e.g. Netcare, ARIA). Knowledge of oncology medical terminology, anatomy and tumor staging. ICH-GCP training and familiarity with clinical trial regulatory reporting requirements. Able to lift and transport large volumes of charts, heavy binders, lab kits, boxes, etc., to various areas on a regular basis. Transfer boxes up to 30 lbs. Push or pull loaded carts. NOTE: To ensure your skills and qualifications are considered, please attach a resume and cover letter with your application.

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
Edmonton AB

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