About the role
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
Ensure the confidentiality of clinical trial participants and sponsors is respected;
Understand protocol driven timed study events and acceptable collection windows (protocol and/or SOP driven) for the timed events;
Report procedural deviations to appropriate supervisory team members;
Preparation and proper clean-up of applicable work-stations (i.e. urine collection station, blood processing station, etc.);
Maintain and advocate a high level of customer service, quality and safety within the department;
Perform clinical trial activities may include but not limited to, sample handling, safety measurements, oral IP administration, and questionnaire administration;
Conduct all clinical trial activities and participant interaction with a high standard of customer service;
Report significant participant misbehavior to Study/Clinical Operations management teams;
Provide feedback, where necessary, to appropriate team members of study progress;
Proactively communicate issues and/or problem resolutions to departmental supervisors and managers;
Complete and/or maintain training as required per jobs needs;
Other tasks as assigned by management.
What you’ll need to succeed
High School Diploma or/and Diploma related to the field of health;
Excellent communication skills in French and English;
Knowledge of another language an asset;
Customer service focused;
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:
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
You must be available full-time during the day for the first 6 to 8 weeks of training.
Variable hours.
Day, evening or night shift (no shift rotation).
On site position at our Montreal site (1200 Beaumont);
Accessible by Public Transportation (Metro L'Acadie), Free Parking for employees.
Altasciences’ Incentive Programs Include:
Training & Development Programs
Employee Referral Bonus Program