Nurse

I R C M•Montreal, QC

5h•Onsite

About The Position

The Montreal Clinical Research Institute (IRCM) is a world-class biomedical research center that puts science to work for health. The work of our teams contributes to major advances in research. We provide an environment where scientific rigor and collaboration drive the advancement of knowledge. Contribute to work that has a tangible impact on health and research. Thrive in a rigorous, collaborative, and supportive environment. Take part in challenging projects and continuous improvement initiatives.

Requirements

Must be a member in good standing of the Ordre des infirmières et infirmiers du Québec (OIIQ).
Must hold a Diploma of College Studies (DEC) in Nursing.
Minimum of 1 year of experience as a registered nurse in a hospital setting.

Nice To Haves

Sound clinical judgment.
Functional bilingualism (French and English).
Skilful in inserting venous catheters and performing blood draws.
Courtesy, empathy, and thoroughness.
Excellent interpersonal and communication skills.
Strong organizational skills and ability to manage multiple tasks simultaneously.
Knowledge of standard software and the electronic medical record system.

Responsibilities

Provide technical nursing support: blood draws, preparation of infusion solutions, insertion of venous catheters and insulin/glucose pump catheters, and performance of adipose tissue needle biopsies (as taught by a physician).
Collect anthropometric and physiological measurements of research participants.
Ensure the continuous assessment, safety, and comfort of patients in the protocols under their responsibility during testing.
Process human biological samples collected during the research protocols.
Compile information and document the scope of interventions in patient records.
Use clinical judgment to manage out-of-protocol situations and consult the on-call physician when needed.
Participate in maintaining the integrity and cleanliness of the clinical/physiology rooms.
Be responsible for the screening and recruiting of eligible participants for the research protocols.
Address the regulatory and ethical aspects related to research projects.
Ensure the clinical follow-up of patients participating in research protocols.
Participate in the entry and verification of clinical data in the laboratory database.
Collaborate with members of the research and the IRCM clinic teams.
Maintain current skills in accordance with the requirements established by the professional order.
Maintain current clinical research training according to the IRCM’s requirements (Good Clinical Practice, Standard Operating Procedures, etc.).
Supervise new team members regarding clinical research protocols.