Research Nurse, Endocrinology Clinical Trials Unit

Research Nurse, Endocrinology Clinical Trials Unit

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The Department of Medicine in the Cumming School of Medicine invites applications for a Fixed Term Recurring Part‑time position. This position is for approximately 12 months (based on length of grant funding), with the possibility of extension.

This role reports to the Team Leader and has accountabilities to the Principal Investigator. The research nurse works within the University and the Clinical Trials Unit within the faculty of Medicine, Endocrinology, primarily at the Clinical Trials Unit in Richmond Road Diagnostic and Treatment Centre. The work environment involves considerable time spent on a computer and interacting with research participants virtually or in the endocrinology unit.

The role will have a substantial impact on the success of the research projects.

The workload will fluctuate according to the protocol and will be approximately 21 hours per week, with strong potential for increased hours. Risks and stress in this position include contact with blood and other body fluids, and exposure to airborne or surface borne diseases.

• Evaluate protocols to develop timelines for conducting and completing the trial
• Work closely with the PI to identify and recruit research participants
• Communicate regularly with the research team (Manager, project manager, PI and sponsor) with study updates, questions and concerns
• Liaise with the supporting technology sponsors to facilitate subject training and provision of equipment
• According to the protocol design, plan and execute study visits, including but not limited to:
  • ensuring materials and supplies are available
  • collecting the required data for each visit and accurately documenting
  • perform study‑related procedures such as assessments and demonstration of new technology (e.g., application of glucose sensor)
  • entering study visit data into the electronic case report form in a timely manner
  • answering data queries or providing source documents to support data as needed
  • communicating regularly with research participants to provide on‑going support (within the expectations of the protocol) and escalating to the PI as needed
  • documenting and communicating adverse event and adverse device events according to the timelines of the protocol, regulatory agencies, REB and the supporting technology sponsors
• Utilize and implement updated study documents as they occur, such as source documents, protocol amendments, informed consent version updates, study directives

• Registered Nurse and current license with College & Association of Registered Nurses of Alberta
• CITI certification in Good Clinical Practice, or equivalent
• Willingness to complete other research training certificates such as Transportation of Dangerous goods, TCPS 2: CORE, and BCLS where relevant to the protocol and act in accordance with the Standard Operating Procedures of the research unit
• Advanced clinical knowledge of diabetes and co‑morbid conditions
• Advanced clinical knowledge of hypertension, obesity and growth hormone deficiency would be assets
• Advanced knowledge, skills and proficiency in diabetes in pregnancy considered an asset
• Advanced knowledge of diabetes technology including glucometers, continuous glucose monitoring systems, and insulin pumps considered an asset
• Expertise with insulin and diabetes medication adjustments an asset
• Experience in interviewing, counseling, teaching and group dynamics
• Demonstrated skills in phlebotomy and processing of biological samples
• Ability to work independently but collaboratively with research participants and team members
• Excellent and effective communication and interpersonal skills
• Leadership and strong organizational skills
• Computer skills to manage study documents, portals, and data entry
• Adherence to the College and Association of Registered Nurses of Alberta Code of Ethics, Policies and Practice of Standards, and applicable legislation to protect human research subjects

January 14, 2026

We would like to thank all applicants in advance for submitting their resumes. Please note, only…