Clinical Trial Quality Control Associate
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Apply clinical data review and quality systems skills as a Clinical Quality Control Associate with Altasciences in Montreal. Work onsite at 1200 Beaumont.
This full-time Clinical Quality Control Associate position supports clinical trial data quality and Quality Systems tasks. You will work under study protocols, Good Clinical Practices, and Standard Operating Procedures. French and English communication, Microsoft Office, and careful data tracking are required.
Key Responsibilities:
- Review clinical trial data for quality control compliance
- Track errors, trends, deviations, and data queries
- Maintain computerized files and deviation tracking systems
- Communicate issues and resolutions to departmental supervisors
- Mentor and coach Quality Systems team members
Requirements:
- Completed high school diploma
- Good communication skills in French and English
- Microsoft Office proficiency
- Strong attention to detail and organization
- Ability to lift up to 25 pounds
Bring clinical data review, confidentiality, and quality systems skills to Altasciences’ onsite Montreal clinical research team.