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Recruits research participants, prescreens patients and obtains informed consent,
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Assesses patients for protocol eligibility through personal interviews and/or medical record review in in-patient and out-patient settings,
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Maintains, completes and updates, concomitant and adverse event logs and questionnaires and protocol specific source documentation,
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Completes patient charting accordingly,
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Coordinates protocol related tests, i.e, venipuncture including sample collection, Pharmacokinetics (PKs), Pharmacodynamics (PDs), urine collection and Electrocardiogram (ECG),
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Processes and shipments of samples according to clinical protocol and manuals,
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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,
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Provides coordination of all aspects of data collection and source documentation,
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Maintains and updates regularly the study lab kit inventory logs, destroys expired kits and requests study kits as needed,
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Schedules site initiation visits, monitoring visits and follows-up with issues identified,
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Acts as a liaison with the radiation and medical oncology groups,
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Conduct other related tasks as assigned by supervisor.
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DEC in sciences or a related field,
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Minimum 1 year of clinical research experience,
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Experience in a hospital/clinical setting is an asset,
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Experience in hematology and/or oncology is an asset,
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Bilingual: French and English spoken and written,
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Critical thinking an asset,
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Solid written and verbal communication skills,
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Autonomous, flexible sense of ethics and good judgment,
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Excellent interpersonal skills,
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Excellent organization, ability to multitasks and prioritize time-sensitive issues,
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Ability to work under minimal supervision,
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Proficiency in MS Office (Word, Excel),
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Clinical research experience is an asset,
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Knowledge of international, federal and provincial laws and regulations governing clinical research (ICH-GCP) is an asset.