Apply clinical data quality control expertise at Altasciences in Montreal, reviewing trial data and supporting Quality Systems tasks onsite.

The Clinical Quality Control Associate reviews clinical trial data and completes quality control activities with the Quality Systems team. This regular full-time position follows study protocols, Good Clinical Practices, and Standard Operating Procedures. The work includes deviation tracking, data queries, issue communication, and confidentiality.

Key Responsibilities:

- Review clinical trial data for quality control
- Report, track, and escalate errors or trends
- Maintain computerized files and deviation tracking systems
- Record, track, and resolve data queries
- Communicate issues and resolutions to supervisors

Requirements:

- Completed high school diploma
- French and English communication skills
- Microsoft Office proficiency
- Robust attention to detail and organization
- Ability to manage conflicting priorities

Support compliant clinical research through careful data review, deviation tracking, communication, and confidentiality at Altasciences Montreal.

📌 Clinical Trial Quality Control Associate (Laval)
🏢 Altasciences
📍 Laval