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Altasciences in Montreal is seeking a Screening Quality Control Associate I to ensure the accuracy, completeness and compliance of all data collected during the screening phase of clinical trials. You will review screening documents, verify participant eligibility, and track data queries to maintain audit-ready data.
This role requires bilingual communication in French and English, strong organizational skills, and the ability to work in a fast-paced environment while upholding GCP and SOP
The Screening Quality Control Associate I is responsible for ensuring the accuracy, completeness, and compliance of all data collected during the screening phase of clinical trials. This role plays a critical part in maintaining data integrity by reviewing screening documentation, identifying discrepancies, and ensuring that all information meets study protocols, Good Clinical Practices (GCP), and Standard Operating Procedures (SOPs). The Screening Quality Control Associate I collaborates closely with the Screening team to support high-quality, audit-ready data throughout the study lifecycle.
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 Screening 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.
On site position at our Montreal office (1100 Beaumont); accessible by public transportation (Metro L'Acadie) and free parking lot for employees. Candidates must be available between 9am and 7pm. Flexibility to work overtime when necessary. Usually one Saturday out of two (sometimes on Sundays).