Clinical Research Coordinator - Urology/CRP (Research Institute)
Clinical Research Coordinator - Urology/CRP (Research Institute)
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Job Description
Do 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 Qubec - Sant (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 service.
General Duties
ROLE:
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.
SPECIFIC RESPONSIBILITIES:
Reviews and analyzes project submissions. Advises on feasibility. Establishes time and cost estimates
Provides technical guidance and assistance concerning work methods the use of equipment and techniques and the analysis of results
Maintains computerized information systems and participates in their development Participate in the development and operation of Biobank databases
Obtain informed consent from participants explain the study and respond to any questions
Collect tissue blood and urine samples from patients
Process collected samples according to standard operating procedures (SOPs) and store them using the Biobanks standardized system
Retrieve stored samples upon request
Extract clinical information from electronic medical records and enter specified data into the Biobank database system
Perform routine database maintenance
Collect clinical data from OACIS (electronic health records) and enter it into REDCap (CBCIS platform)
Screen patient lists to determine CBCIS (Canadian Bladder Cancer Information System) eligibility review medical records and extract relevant data for CBCIS entry
Perform annual follow-ups for enrolled CBCIS subjects and ensure their records and status are accurately updated in the system
Complete all other relevant duties as assigned by the supervisor or principal investigator (PI)
Accomplishes any other tasks as required by the immediate supervisor.
Website of the organization
Required Skills
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 problem-solving 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).
Additional information
Status: Temporary full time (35-hour workweek)
Pay Scale: Commensurate with education and experience. $44408.00 - $82427.80.
Work Shift: 8:00 am to 4:00 pm
Work Site: Glen site
***If you wish to include a cover letter please attach it with your resume in one PDF document. ***
Why work with us
4-week vacation 5th week after 5 years
Bank of 12 paid days (personal days and days for sickness or family obligations)
13 paid statutory holidays
Modular group insurance plan (including gender affirmation coverage)
Telemedicine
RREGOP (defined benefit government pension plan)
Training and professional development opportunities
Child Care Centres
Corporate Discounts (OPUS Perkopolis)
Competitive monthly parking rate
Employee Assistance Program
Recognition Program
Flex work options and much more!
learn more about our benefits please visit IS NOT A HOSPITAL POSITION.
Equal Opportunity Employment Program
The Research Institute of the McGill University Health Centre hires on the basis of merit and is strongly committed to equity diversity and inclusion within its community. We welcome applications from all qualified candidates who self-identify as members of racialized groups/visible minorities women Indigenous persons persons with disabilities ethnic minorities and 2SLGBTQIA persons. We also welcome candidates with the skills and knowledge to productively engage with diverse communities. Persons with disabilities who anticipate needing accommodations for any part of the application process may confidentially contact
Required Experience:
IC
Employment Type
Full-Time
