Clinical Research Coordinator – Nurse CIM Oncology (Research Institute)
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Job Location:
Monthly Salary:
Posted on:
30+ days ago
Vacancies:
1 Vacancy
Job Summary
Organization description
Le Centre universitaire de santé McGill (CUSM) est un centre hospitalier universitaire intégré reconnu à léchelle internationale pour lexcellence de ses programmes cliniques de sa recherche et de son enseignement. Le CUSM a pour objectif dassurer aux patients des soins fondés sur les connaissances les plus avancées dans le domaine de la santé et de contribuer au progrès des connaissances.
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
Under the supervision of the Manager of Oncology Research Centre for Innovative Medicine (CIM) the Clinical Research Coordinator Nurse is responsible for supporting the successful conduct of clinical research studies in oncology. The incumbent will collaborate with Investigators and health care personnel to assume responsibility for overall patient management and the coordination of several clinical studies for the CIM-Oncology Department of the RI-MUHC.
The Centre for Innovative Medicine is located in the new Glen site hospital which is a unique center in Canada of 5000 m2 dedicated exclusively to clinical research.
General Duties
Obtains informed consent assesses patients for protocol eligibility through personal interviews and/or medical record review in in-patient and out-patient settings
Maintains and completes concomitant medication adverse events and questionnaires logs forms and protocol specific source documentation
Monitors patient safety and medication compliance
Prepares orders for protocol related requests and procedures consults prescriptions requests for pathology slides and blocks as needed
Coordinates all aspects of data collection and source documentation
Completes all research related documents and responds to queries and requests for information
Conducts protocol specific and scientific trainings
Creates protocol specific nursing alerts/feasibilities for the oncology day center
Responsible for assisting with the submission of serious adverse events to the Research Ethics Board
Conduct other related tasks as assigned by supervisor.
Required Skills
Bilingual: French and English spoken and written in order to communicate efficiently with patients and personnel
Solid written and verbal communication skills
Able to work under minimal supervision
Self-directed flexible organized and sense of ethics
Knowledge of international federal and provincial laws and regulations governing clinical research (ICH-GCP) is an asset.
Required Experience:
IC
Key Skills
- Clinical Research
- FDA Regulations
- Data Collection
- GCP
- Infusion Experience
- Phlebotomy
- Clinical Trials
- Pediatrics Experience
- Qualitative Research Interviewing
- Research Experience
- Nursing
- Epic
About Company
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