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) (Ontario)
🏢 PSI CRO
📍 Ontario