Join a dedicated team as a Freelance Clinical Research Associate with a focus on Oncology. This role will enhance your skills in monitoring and regulatory processes across Canada. We're looking for an experienced CRA to oversee site monitoring, conduct visits, and ensure compliance with clinical study guidelines. As a vital member of the team, you will engage in feasibility studies and communicate closely with various stakeholders. Fluency in both English and French is essential for this position. Key Responsibilities:
Plan and conduct site monitoring visits, documenting findings
Verify source documents and review CRFs for accuracy
Manage communications between sites and in-house teams
Assist in preparing for audits and inspections
Support the regulatory team with necessary submissions Requirements:
Degree in Life Sciences or related experience
Previous experience in Phase II and/or III monitoring
Oncology experience is a plus
Full proficiency in English and French
Able to travel and possess a valid driver’s license Make your mark in clinical research and advance patients' lives through creative studies. #J-18808-Ljbffr

📌 Freelance Clinical Research Associate Oncology Focus Toronto
🏢 PSI CRO
📍 Toronto