Senior Clinical Research Associate

📋 Description

• Travel to clinical trial sites as required to support monitoring and study activities.
• Conduct and document Site Initiation Visits (SIV), Routine Monitoring Visits (RMV), and Close-Out
• Review Case Report Forms, perform source data verification, and manage queries.
• Coordinate with internal teams and external vendors to deliver studies on time.
• Communicate study progress, risks, issues, and site updates to project teams.
• Support feasibility assessments and site selection activities.

🎯 Requirements

• College or university degree in Life Sciences or equivalent experience.
• Proven experience conducting independent on-site clinical monitoring.
• Hands-on monitoring in Phase II and/or Phase III trials.
• Experience in oncology clinical research is a plus.
• Full professional proficiency in English with strong communication skills.
• Proficiency with MS Office and maintaining accurate documentation.

🎁 Benefits

• Freelance opportunity supporting clinical research activities across Canada.
• Opportunity to develop clinical monitoring and study management expertise.
• Exposure to Phase II and Phase III trials across therapeutic areas.
• Broaden oncology experience and therapeutic-area knowledge.
• Collaboration with experienced clinical research, regulatory, and project teams.
• Exposure to feasibility activities, regulatory submissions, audits, and inspections.