Clinical Research Coordinator - Montréal, Canada - Centre universitaire de santé McGill
Description
Organization descriptionLe Centre universitaire de santé McGill (CUSM) est un centre hospitalier universitaire intégré, reconnu à l'échelle internationale pour l'excellence de ses programmes cliniques, de sa recherche et de son enseignement.
Le CUSM a pour objectif d'assurer 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 direction of the immediate supervisor, oversees the day-to-day operations of a facility, a large laboratory or several laboratories.
Organizes, distributes and verifies the work of others and participates in their training. Establishes priorities and schedules of projects. Coordinates execution of projects and serviceGeneral Duties
Under the direction of the immediate supervisor, the incumbent will:
- Oversees the day-to-day operations of the laboratory,
- Coordinates the execution of experiments, projects and services,
- Establishes priorities and ensures adherence to schedules,
- Ensures efficiency and quality of output,
- Performs accounting functions such as monitoring expenditures, verifying ledgers and resolving discrepancies. Forecasts costs of supplies, materials and equipment. Prepares invoices. Prepares budgets or budget proposals.
Education / Experience
Education:
Diploma of College Studies (DEC)
Field of Study:
DEC in related field
Work Experience:
Two (2) years of related experience
Professional Membership:
- Yes No
Other Requirements:
- Excellent French and English, spoken and written,
- Excellent communication and interpersonal skills,
- Ability to work independently or with teams with minimum supervision,
- Ability to generate and maintain accurate records,
- Strong analytical and problemsolving skills,
- Decision making: Planning, implementing and evaluating patient care. While the investigator is the main responsible for his/her study, the incumbent must ensure protocol compliance including participant eligibility,
- Clinical research experience is an asset,
- Knowledge of Microsoft Office (Word, Excel, Power Point and Outlook).
Status:
Temporary Full-Time (35-hour workweek)
Pay Scale:
$42,260.40 to $48,000.00, commensurate with education and experience
Work Shift: 8:00 AM to 4:00 PM
Work Site:
Glen
THIS IS NOT A HOSPITAL POSITION.
Equal Opportunity Employment Program
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