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Clinical Research Nurse

2 months ago


Montreal, Quebec, Canada Centre de recherche de l\'Hôpital Maisonneuve-Rosemont Full time

Job Summary

The Clinical Research Nurse will work under the supervision of Dr. Richard LeBlanc in the Myeloma Multiple Research Team at the Centre de recherche de l'Hôpital Maisonneuve-Rosemont. In collaboration with hematologists and clinical research unit members, this nurse will participate in various levels of studies from local researchers and pharmaceutical companies.

The successful candidate will be responsible for recruiting, following up, and caring for participants to ensure their safety while respecting research protocol requirements, hospital procedures, and clinical best practices. They will also be involved in data collection related to research projects.

The research team's mission is to improve patient care, innovate through research, and promote knowledge dissemination on various aspects related to multiple myeloma. Our dynamic team works to improve survival and quality of life for patients with this disease.

Main Responsibilities

  • Participate in activities related to study requirements (study setup, participant recruitment, treatment visits, follow-up visits, data collection, data entry, etc.) according to the protocol and local and international regulations to achieve the highest quality standards.
  • Participate in the smooth conduct of medical visits (complete information from source documents, ensure clinical follow-up of patients, etc.).
  • Coordinate and execute the various tests required by the protocol (blood draws, vital signs, medication distribution for the study, etc.) and follow up on appointments with different services.
  • Act as a resource person for research subjects to explain the different stages of the project they are participating in while responding to their questions and expectations.
  • Review medical records.
  • Enter data into various electronic systems and ensure that the information is complete before the regular surveillance visit.
  • Collaborate and interact with pharmaceutical companies and contract research organizations (CROs).
  • Participate in project meetings to maintain high-quality standards.

Consult the complete job offer PDF