Research I

Avenue.io Inc.; Edmonton; On-site; CAD 53,000 - 70,000; Full time

Job summary

AHS Clinical Trials Unit in Edmonton is recruiting a Research Coordinator to support Investigators in GI and Liver trials at the University of Alberta. You will manage study activities, screen participants, obtain informed consent, and coordinate scheduling of visits and procedures.

You will develop study documents, review lab results and reports, maintain training records, and contribute to education for participants.

Qualifications

• Minimum 4-5 years of hands-on experience in pharmaceutical clinical research (Phases I–IV).
• Experience supporting Hepatology and Gastroenterology trials.
• Proficiency with EDC systems and clinical trial databases.

Responsibilities

• Screen potential participants and obtain informed consent.
• Coordinate enrollment, retention, follow-up activities and scheduling.
• Maintain accurate study documentation and regulatory compliance.

Skills

Clinical research coordination

Informed consent

Participant management

ICH-GCP knowledge

EDC systems

Education

Diploma or degree in health or science

Tools

iMedidata

Connect Care

Netcare

Microsoft Excel

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.