Clinical Research Coordinator, Oncology Research (Research Institute)
Clinical Research Coordinator, Oncology Research (Research Institute)
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Job Description
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 supervision of the Manager of Oncology Research Centre for Innovative Medicine (CIM) the Oncology Clinical Research Coordinator is responsible for supporting the successful conduct of clinical research studies in oncology. The Clinical Research Coordinator collaborates with Investigators and health care personnel to assume responsibility for the overall patient management and coordination of several clinical studies for the CIM-Oncology Department of the RI-MUHC.
The Centre for Innovative Medicine is located in the new Glen site hospital which is a unique center in Canada of 5000 m2 dedicated exclusively to clinical research.
Duties
Recruits research participants prescreens patients and obtains informed consent
Assesses patients for protocol eligibility through personal interviews and/or medical record review in in-patient and out-patient settings
Maintains completes and updates concomitant and adverse event logs and questionnaires and protocol specific source documentation
Completes patient charting accordingly
Coordinates protocol related tests i.e venipuncture including sample collection Pharmacokinetics (PKs) Pharmacodynamics (PDs) urine collection and Electrocardiogram (ECG)
Processes and shipments of samples according to clinical protocol and manuals
Create study specific source documentation i.e study visits AE and Conmed logs study imaging forms pathology request forms ICF tracking log prior to study activation and other study related forms
Provides coordination of all aspects of data collection and source documentation
Maintains and updates regularly the study lab kit inventory logs destroys expired kits and requests study kits as needed
Schedules site initiation visits monitoring visits and follows-up with issues identified
Acts as a liaison with the radiation and medical oncology groups
Conduct other related tasks as assigned by supervisor.
Website of the organization
Required Skills
Exhibits strong interpersonal and organization skills
Ability to take initiative work under pressure manage multiple projects and priorities
Ability to pay attention to detail
Ability to generate and maintain accurate records
Ability to draft communications and correspondence in French and English
Excellent verbal and written communications skills in French and English
Bilingual: French and English spoken and written
Critical thinking an asset
Solid written and verbal communication skills
Autonomous flexible sense of ethics and good judgment
Excellent interpersonal skills
Excellent organization ability to multitasks and prioritize time-sensitive issues
Ability to work under minimal supervision
Proficiency in MS Office (Word Excel)
Clinical research experience is an asset
Knowledge of international federal and provincial laws and regulations governing clinical research (ICH-GCP) is an asset.
Required Experience:
IC
Employment Type
Unclear
