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RI-MUHC | Research Institute of the MUHC | #rimuhc logo

Clinical Research Coordinator, Phase 1 (Research Institute)

Verified
Montreal, QC
CA$44,408 - CA$82,427/year
Entry Level
Full-time

Top Benefits

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

About the role

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 Phase 1 Research at the Centre for Innovative Medicine (CIM), the Clinical Research Coordinator is responsible for supporting the successful conduct of clinical research studies. The person will collaborate with Investigators and health care personnel to assume responsibility for the overall patient management and coordination of several clinical studies for the RI-MUHC.

The Centre for Innovative Medicine is located in the Glen site hospital, which is a unique center in Canada of 5000 m2 dedicated exclusively to clinical research.

More information on the CIM: http://rimuhc.ca/web/research-institute-muhc/centre-for-innovative-medicine

General Duties

• Recruits research participants, prescreens patients and obtains informed consent, assesses patients for protocol eligibility through personalized interviews and/or medical record review in in-patient and out-patient settings,

• Maintains and completes (either in paper or electronic formats) medication, adverse events and questionnaires logs, forms and protocol specific source documentation, ensures ethical approvals are continued throughout the study,

• Monitors patient safety and medication compliance,

• Completes all follow-ups as per special protocol requirements: patient visits/status, disease site active trial lists and completes clinical notes,

• Coordinates orders for protocol related requests and procedures: consultations, requests for pathology, diagnostic and analytical laboratories, etc,

• Coordinates all aspects of data collection and source documentation,

• Completes all research related documents and responds to queries and requests for information,

• Collaborates and acts as a liaison with the various departments within the Research Institute and the MUHC as well external parties,

• Conduct other related tasks as assigned by the Supervisor/Manager.

Education / Experience

Education: Diploma of College Studies (DEC)

Field of Study: Science

Work Experience: 2 years

Required Skills

• Excellent French and English, spoken and written,

• Excellent communication and interpersonal skills,

• Ability to work independently or with teams with minimum supervision,

• Self-directed, flexible, organized and sense of ethics and compliance,

• Experience with pediatric population is an asset,

• Knowledge of regulations governing clinical research (ICH-GCP), H-C, FDA is an asset.

About RI-MUHC | Research Institute of the MUHC | #rimuhc

Research Services
501-1000

The Research Institute of the McGill University Health Centre (The Institute) brings together pediatric and adult research programs, accelerating the translation of biomedical research to improve human health.