Found Description
Be part of the future of cancer treatment with Translational Research in Oncology (TRIO) as a remote Clinical Research Associate. This part-time freelance role focuses on monitoring oncology trials while ensuring compliance with industry standards.
TRIO is looking for a dedicated Clinical Research Associate to join their Monitoring Resource team on a 6-month contract. Candidates should have at least 2 years of monitoring experience in oncology trials, possess a science-related Bachelor’s degree, and be fluent in both French and English. You will be responsible for data verification and site visits, ensuring adherence to FDA and ICH-GCP guidelines.
Key Responsibilities:
• Verify source document data accurately
• Conduct pre-study, initiation, and monitoring site visits
• Ensure compliance with FDA and local regulations
• Assist in budget negotiation and follow-up
• Mentor junior team members as needed
Requirements:
...
TRIO is looking for a dedicated Clinical Research Associate to join their Monitoring Resource team on a 6-month contract. Candidates should have at least 2 years of monitoring experience in oncology trials, possess a science-related Bachelor’s degree, and be fluent in both French and English. You will be responsible for data verification and site visits, ensuring adherence to FDA and ICH-GCP guidelines.
Key Responsibilities:
• Verify source document data accurately
• Conduct pre-study, initiation, and monitoring site visits
• Ensure compliance with FDA and local regulations
• Assist in budget negotiation and follow-up
• Mentor junior team members as needed
Requirements:
...
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