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RM
Infection Control Practitioner
Ross Memorial Hospital
Kawartha Lakes, ON · Lindsay, ON
- Temporary
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Quality Specialist LNG
Airswift
Kitimat, BC
- Contract
Support implementation of project quality management systems and quality plans.
Added 5 mins ago
VT
Business Systems Analyst
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Toronto, ON
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- $25 CAD / hour
- Contract
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- $60 to $95 CAD / hour
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Senior level (minimum 5 years UX and UI experience) with strong expertise in building Design Systems and Figma to support the Trade platform
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Added 5 mins ago
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Indoor Merchandiser
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…Office before execution, and proactively manages changes to support reliable…
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Account Manager, Customer Lifecycle (BC & Alberta)
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- $55,000 CAD / year
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You will proactively engage customers to understand their business and technology needs, support the adoption of Cansel solutions, and identify opportunities to strengthen and expand each…
Added 21 mins ago
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Account Manager, Customer Lifecycle (Ontario & Quebec)
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- $55,000 CAD / year
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Added 21 mins ago
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Account Manager - Subsurface Technologies Equipment (Western Ontario)
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Added 21 mins ago
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Added 21 mins ago
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Assistant Store Manager - Promenades St-Bruno
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Alberta Health Services

Research I

AB, Canada
Edmonton, AB, Canada

Classification: Research I Union: HSAA Facility PROF/TECH Unit and Program: Clinical Trial Unit Primary Location: U of A Hospital Location Details: As Per Location Multi-Site: Not Applicable FTE: 1.00 Posting End Date: 10-NOV-2026 Employee Class: Regular Full Time Date Available: 14-DEC-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: $38.80 Maximum Salary: $51.16 Vehicle Requirement: Not Applicable · Full-time

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Job details

Pay: Classification: Research I Union: HSAA Facility PROF/TECH Unit and Program: Clinical Trial Unit Primary Location: U of A Hospital Location Details: As Per Location Multi-Site: Not Applicable FTE: 1.00 Posting End Date: 10-NOV-2026 Employee Class: Regular Full Time Date Available: 14-DEC-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: $38.80 Maximum Salary: $51.16 Vehicle Requirement: Not Applicable
Job type: Full-time
Apply by: Dec 3, 2026
Posting language: English
Posted: Nov 3, 2026

Original job description

Your Opportunity:

The AHS Clinical Trials Unit is recruiting a Research Coordinator to provide support to Investigators for clinical research trials. You will be assigned to the Gastrointestinal and Liver Disease Research Group (GILDR). The Division of Gastroenterology’s Gastrointestinal and Liver Research Group (GILDR) is a leading North America clinical research centre focused on gastrointestinal and liver clinical trials located at the University of Alberta. The primary responsibility of this position is study management, including the screening and recruitment of potential study participants, providing patient care, obtaining informed consent, and completing protocol-specific assessments and scheduling appointments and procedures. Development of study-specific source documents and ensuring that all relevant documentation, such as laboratory results and hospital diagnostic reports are received, reviewed, and maintained appropriately. In addition, the role involves providing education to participants enrolled in clinical research studies regarding study protocols, treatment visit schedules, and the use of study-related data collection tools. The individual is responsible for ensuring completion of all required training on study procedures and maintaining accurate and timely documentation of such training. There may be an opportunity for mentorship and guidance to support the development of knowledge and experience in GILDR’s day-to-day research operations. As the individual’s skills and experience develop, there may be opportunities to take on additional responsibilities in support of operational activities, team needs and ethics applications.

Description:

As a Research I, you will be working with research teams which are generating and disseminating new knowledge that assists with advancing the understanding of health disciplines and various health and medical concerns. Working under the guidance of the principal investigator, you will be responsible for preparing and submitting research documents, collecting and reviewing a variety of information related to the study, and monitoring study compliance. You will also assist with the recruitment of study participants and initiate consenting of study and/or trial participants and may complete lab work to support research activities.

Classification: Research I Union: HSAA Facility PROF/TECH Unit and Program: Clinical Trial Unit Primary Location: U of A Hospital Location Details: As Per Location Multi-Site: Not Applicable FTE: 1.00 Posting End Date: 10-NOV-2026 Employee Class: Regular Full Time Date Available: 14-DEC-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: $38.80 Maximum Salary: $51.16 Vehicle Requirement: Not Applicable

Required Qualifications:

Diploma or degree in a health or science related field. Registration with applicable professional association or college where required.

Additional Required Qualifications:

Minimum 4-5 years of current hands on experience in pharmaceutical clinical research, supporting (Phases I–IV) clinical trials in Hepatology and Gastroenterology therapeutic research. Proven expertise in all aspects of study coordination and participant management, including pre-screening, screening, patient recruitment, informed consent, enrollment, retention, and follow-up activities. Comprehensive knowledge of clinical trial regulations and guidelines, including ICH-GCP, Health Canada, and FDA requirements. Proficiency in electronic data capture (EDC) systems and clinical trial databases, including iMedidata. Skilled in standard computer applications (Microsoft Excel, Word, PowerPoint). Experience using Connect Care and Netcare. Proven ability to perform diversified duties requiring independent judgment, discretion, and confidentiality. Strong problem-solving, critical thinking, and organizational skills with the ability to manage multiple priorities and tight timelines and accept new workloads as necessary. Must be able to lift and transport large volumes of charts, binders, lab kits, boxes etc. to various areas on a regular basis, and push/pull loaded carts. Physical demands of the job include sitting for extended periods, lifting and transporting office/medical supplies and equipment weighing up to 40 lbs., and using repetitive motions, lifting, bending, reaching and standing for prolonged periods.

Preferred Qualifications:

Due to the specialized nature of clinical investigational drugs and procedures, you will require extensive knowledge on the agents, mechanisms of action, and their adverse event profiles. This requires being able to explain difficult, complex information to patients and ensure their understanding to obtain informed consent.

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More about this job

Responsibilities

Coordinate gastrointestinal and liver clinical trials, including screening, recruiting, consenting, enrolling, and following up with participants, as well as providing study-related education and care. Prepare and maintain study documents, review study information and records, schedule assessments and procedures, and monitor compliance with protocols and training requirements.

Requirements

Requires a diploma or degree in a health- or science-related field and, where applicable, registration with a professional association or college. Requires 4–5 years of current hands-on pharmaceutical clinical research experience supporting Phase I–IV trials in hepatology and gastroenterology, knowledge of clinical trial regulations, and proficiency with EDC systems, iMedidata, Microsoft Office, Connect Care, and Netcare.

Skills

Clinical Trial Coordination
Participant Screening and Recruitment
Informed Consent
Participant Enrollment and Retention
Clinical Trial Compliance
ICH-GCP
Health Canada and FDA Regulations
Electronic Data Capture
iMedidata
Microsoft Excel
Microsoft Word
Microsoft PowerPoint
Connect Care
Netcare
Study Documentation
Patient Education

Visa sponsorship

Not detected in the job text

Keywords

Clinical Research
Clinical Trials
Gastroenterology
Hepatology
Liver Disease
Phase I–IV Trials
Study Coordination
Participant Screening
Patient Recruitment
Informed Consent
Participant Enrollment
Participant Retention
Follow-Up
ICH-GCP
Health Canada Requirements
FDA Requirements
Electronic Data Capture
iMedidata
Clinical Trial Databases
Microsoft Excel
Microsoft Word
Microsoft PowerPoint
Connect Care
Netcare
Study Documentation
Protocol Compliance
Ethics Applications
Adverse Event Profiles
Patient Education

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