The Clinical Research Technician will work with Clinic teams to execute clinical trial activities. Responsibilities of the Clinical Research Technician include execution of tasks performed/clinical activities in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOP)s. Please note that this is a variable status position.
What you’ll do here
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Ensure the confidentiality of clinical trial participants and sponsors is respected;
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Understand protocol driven timed study events and acceptable collection windows (protocol and/or SOP driven) for the timed events;
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Report procedural deviations to appropriate supervisory team members;
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Preparation and proper clean-up of applicable work-stations (i.e. urine collection station, blood processing station, etc.);
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Maintain and advocate a high level of customer service, quality and safety within the department;
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Perform clinical trial activities may include but not limited to, sample handling, safety measurements, oral IP administration, and questionnaire administration;
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Conduct all clinical trial activities and participant interaction with a high standard of customer service;
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Report significant participant misbehavior to Study/Clinical Operations management teams;
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Provide feedback, where necessary, to appropriate team members of study progress;
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Proactively communicate issues and/or problem resolutions to departmental supervisors and managers;
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Complete and/or maintain training as required per jobs needs;
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Other tasks as assigned by management.
What you’ll need to succeed
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High School Diploma or/and Diploma related to the field of health;
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Excellent communication skills in French and English;
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Knowledge of another language an asset;
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Customer service focused;
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Able to work in fast-paced environment.
Altasciences strives to provide a French working environment for its employees in Quebec. Although as part of its francization program has taken all reasonable steps to avoid imposing the above-mentioned requirement. Fluency in English is an essential requirement for the position of Clinical Research Technician including, but not limited to, for the following reasons:
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The requirement to have study protocols, designs and clinical research documents written and documented in English as required by industry regulatory agencies.
What we offer
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You must be available full-time during the day for the first 6 to 8 weeks of training.
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Variable hours.
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Day, evening or night shift (no shift rotation).
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On site position at our Montreal site (1200 Beaumont);
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Accessible by Public Transportation (Metro L’Acadie), Free Parking for employees.