Clinical Research Coordinator

3 weeks ago

Montréal, Canada Centre universitaire de santé McGill Full time

Organization description

Le 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 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 which 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,
- 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,
- Excellent communication and interpersonal skills,
- Problem-solving skills,
- 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 —One-year renewable contract

**Pay Scale**: $42,260.40 to $78,460.20, commensurate to qualifications and experience

**Work Shift**: 8 AM to 4 PM, Monday to Friday (35 hours)

**Work Site**: Glen site (1001 Decarie Blvd, Montreal)

THIS IS NOT A HOSPITAL POSITION.
Equal Opportunity Employment Program

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