Elevate your career as a Senior Clinical Research Associate with a global leader in medical science based in Canada. This freelance position focuses on critical monitoring and site management tasks.

As a Senior CRA with our mid-sized company, you will play a vital role in conducting SIV, RMV, and COV onsite monitoring visits. You'll oversee site communications, resolving queries effectively while collaborating with internal and external teams. Your skills in CRF review will ensure high standards in study operations and compliance.

Key Responsibilities:
• Perform onsite monitoring for clinical trials
• Verify source documents and resolve queries
• Communicate with internal teams about study updates
• Liaise with vendors and provide support services
• Assist regulatory team with study documentation and audits

Requirements:
• College/University degree in Life Sciences
• Proven experience in Phase II and/or II...