Clinical Research Coordinator- - Edmonton, Canada - Alberta Health Services

Alberta Health Services

Verified Company

Edmonton, Canada

1 week ago

Posted by:

Sophia Lee

beBee Recruiter

Description

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.

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: 03-JAN-2023

Temporary Employee Class: Temp F/T Benefits

Date Available: 23-JAN-2023

Temporary End Date: 27-OCT-2023

Hours per Shift: 7.75
Length of Shift in weeks: 2
Shifts per cycle: 10
Shift Pattern: Days
Days Off: Saturday/Sunday
Minimum Salary: $31.71
Maximum Salary: $40.40
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:

Phase 1 trials experience is an asset. Prior experience working with pharmaceutical sponsors. An ability to multi-task effectively in a busy area with multiple interruptions and competing demands. Knowledge of oncology medical terminology, anatomy and tumor staging. ICH-GCP training and familiarity with clinical trial regulatory reporting requirements. Excellent computer skills and experience working with Microsoft Office programs. Familiar with using and creating spreadsheets, and using various databases (e.g. InForm, RAVE). Experience with electronic medical records (e.g. Netcare, ARIA, ConnectCare), and ethics submission systems (IRISS, REMO).

Must be able to transport large volumes of materials (study supplies, charts, boxes, etc.) to various areas regularly and push/pull loaded carts.

Physical demands of the job include sitting for extended periods, lifting office/medical supplies and equipment weighing up to 30 lbs., and using repetitive motions, lifting, bending, reaching and standing for prolonged periods.

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.