Clinical Research Coordinator (research Institute)

Montreal, QC, Canada

Job Description


Job Number:

J0124-0260

Job Title:

Clinical Research Coordinator (Research Institute)

Organisation:

Research Institute of the MUHC

Work Location:

SITE GLEN

Job Category:

Research and teaching

Job Type:

Temporary full time

Salary:

$42,260.40 - $78,460.20 /Year

Shift:

Day

Open Positions:

1

Le Centre universitaire de sant\xc3\xa9 McGill (CUSM) est un centre hospitalier universitaire int\xc3\xa9gr\xc3\xa9, reconnu \xc3\xa0 l\'\xc3\xa9chelle 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 fond\xc3\xa9s sur les connaissances les plus avanc\xc3\xa9es dans le domaine de la sant\xc3\xa9 et de contribuer au progr\xc3\xa8s des connaissances.



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 Qu\xc3\xa9bec - Sant\xc3\xa9 (FRQS).

Position summary
Under the general supervision of the principal investigator and/or the supervisor and in close collaboration with the study team and study sub-investigators, the incumbent is responsible for the coordination of clinical research studies.

The clinical research coordinator will collaborate with all members of the project team and will be responsible for the overall general coordination and follow up of the study participants.

General Duties

  • Coordinates study initiation and study visits,
  • Recruits research participants,
  • (Preferred but not required): takes blood samples of participants,
  • Obtains blood and other biofluid samples and organizes their transfer to the analysis site,
  • Process samples (e.g., centrifugation and other protocols) and biobank,
  • Acts as the direct link between the investigator, the research team and collaborating laboratories/co-investigators,
  • Acts as the primary contact for the investigator\'s team concerning clinical research and external sites,
  • Planning, implementation and maintaining of data collection and analysis systems according to the research protocol,
  • Collection and storing of questionnaires, consent forms and participants\' study files,
  • Ensures the timely completion of all study documents, including case report forms and other study-specific documents,
  • Assists in the development of protocols, consent forms, questionnaires and other study documents,
  • Assists with ethic submissions and amendments,
  • Assists in the preparation and submission of abstracts and manuscripts,
  • Conducts literature reviews and keeps current with study literature,
  • Designs and maintains databases and online surveys,
  • Manages accounts and transfers of funds,
  • The list of duties and responsibilities outlined above is representative and not a complete and detailed list of tasks that may be performed by an employee whose position has been matched to this generic job description.
Website of the organization

Education / Experience

Education: DEC

Field/Discipline: Medical Technology or any related field such as Nursing or sciences

Experience: 2 years

Order: OPTMQ standing member is preferred

Additional information:
  • A minimum of two years of clinical research experience in an academic environment or/and in a clinical research organization required,
  • Bilingual, French and English (proficient reading and writing),
  • Experience in (research) project coordination, an asset,
  • Knowledge of data storage and analysis systems, an asset,
  • Strong proficiency in Microsoft Office programs (Word, Excel, PowerPoint) and web applications,
  • Excellent communication and interpersonal skills,
  • Problem-solving skills,
  • Ability to work well with co-workers, peers, monitors and potential subjects and have a positive demeanor,
  • Willingness to acquire new skills and adapt to new situations,
  • Must be professional, possess a high degree of efficiency and self-motivation, and have a strong work ethic and respect for confidentiality.
Additional information

Status: Full-time (35-hour workweek) - One-year renewable contract
Pay Scale: Commensurate to qualifications and experience, $42,260.40 - $78,460.20
Work Shift: 8 a.m. to 4 p.m., Monday to Friday
Work Site: Glen site

https://rimuhc.ca/careers

To learn more about our benefits, please visit

THIS 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,

McGill University Health Centre

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Job Detail

  • Job Id
    JD2272719
  • Industry
    Not mentioned
  • Total Positions
    1
  • Job Type:
    Full Time
  • Salary:
    $42260.4 - 78460.2 per year
  • Employment Status
    Permanent
  • Job Location
    Montreal, QC, Canada
  • Education
    Not mentioned