About The Role The Clinical Quality Control Associate is responsible for the quality control (QC) review of clinical trial data and working with the Quality Systems team to complete QC related tasks. The Clinical Quality Control Associate will conduct tasks performed within compliance of study protocol, Positive Clinical Practices (GCP) and Standard Operating Procedures (SOPs).
What You'll Do Here Report, track and elevate (if necessary) errors and/or trends that may require re-training, as required by location.
Compile data and maintain computerized files and/or update deviation tracking systems.
Record, track and ensure the resolution of data queries.
Proactively communicate issues and/or problem resolutions to departmental supervisors and managers.
Ensure the confidentiality of clinical trial participants and sponsors is respected.
Maintain and advocate a high level of quality and customer service within the department.
May document and/or report clinical trial related deviations (i.e. SOP, protocol).
Act as a mentor and coach the Quality Systems team members.
Understand protocol driven timed study events and acceptable collection windows (protocol and/or SOP driven) for the timed events.
Other tasks as assigned by management.
What You'll Need to Succeed High School Diploma completed.
Related work experience an asset.
Good Communication in French and English.
Detail oriented, well organized, customer service focused, able to work in fast-paced workplace.
Software: Microsoft Office.
Strong attention to details




Personal/professional integrity and proven discretion in handling confidential information.
Ability to develop strong trusting relationships in order to gain support and achieve results.
Capable of managing multiple conflicting priorities.
Must be self-directed, motivated and have a willingness to take initiative.
The candidate must be able to lift up to 25 pounds.
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 Quality Control Associate 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 Regular full-time position; 37.5 hours a week.
Candidate needs to be available between 7am and 7pm and 1 every 3 week-ends.
On site, Montreal site (1200 Beaumont).
Accessible by metro (L'Acadie); Free parking for employees.
Altasciences benefits Health/dental/vision insurance plans
RRSP with employer match
Paid vacation and statutory vacations
Paid sick leave and bereavement leave
Employee assistance and telehealth programs
Altasciences incentive programs include Training and development programs
Employee orientation bonus program
Annual performance reviews

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📌 Clinical Quality Control Associate II (Quebec City)
🏢 Altasciences
📍 Quebec City