Clinical Research Nurse Coordinator (Research Institute)
Research Institute of the McGill University Health CentreMontréal, CADo you want to work for a world-renowned research institute that pushes the boundaries of biomedical science and health research? Right here in Montreal! At the Research Institute of the McGill University Health Centre (RI-MUHC), you can be part of an organization focused on scientific discovery and innovation in patient-centered medicine. Join us today and make a difference!
Job Description
RESEARCH INSTITUTE OF THE MUHC
The Research Institute of the McGill University Health Centre (RI-MUHC) is a world-renowned biomedical and hospital research centre. Located in Montreal, Quebec, the Institute is the research arm of the McGill University Health Centre (MUHC) affiliated with the Faculty of Medicine at McGill University. The RI-MUHC is supported in part by the Fonds de recherche du Québec - Santé (FRQS).
Position summary
The incumbent will be involved with clinical research in gastroenterology and more specifically inflammatory bowel disease (IBD). Document and data management is an essential part of this position. The incumbent will work closely with research team, IBD physicians as well as with gastroenterology nurses mainly on clinical study protocols.
The person will also help to initiate industry sponsored clinical trials including assisting with REB documents, coordination, regulatory work, advertising, and accounting.
General Duties
- Follow-up of patients included in clinical trials, including administration of study drugs and care coordination,
- Processes and prepares biological samples for international shipment,
- Completes source documents and electronic case report forms,
- Identify potential patients and obtain their consent,
- Completes and maintains up-to-date specific trainings,
- Collaborates and assists team members and sponsors’ representatives,
- Reviews study protocols and informed consent forms,
- Contacts patients and their families as needed,
- Screens and collects medical charts of eligible patients,
- Assists Senior research staff with the ethics and regulatory tasks,
- Completes of all other connected tasks as assigned by supervisor,
- Complies with Good clinical practice standards (GCP).
STANDARDS OF PERFORMANCE :
Website of the organization
Education / Experience
Diploma of College Studies (DEC)
Field of Study : Nursing
Work Experience : Experience in research will be considered an asset
Professional Membership : ☒ Yes ☐ No
If yes, please specify : OIIQ
Other Requirements :