Lead Clinical Research Associate

📋 Description

• Oversee site management activities and start-up processes for global clinical trials.
• Coordinate investigator/site feasibility, site identification, and monitoring activities.
• Lead country-level project teams and ensure data integrity, regulatory compliance, and risk
• Mentor monitors and Lead CRAs; support investigator training initiatives.
• Collaborate with internal/external stakeholders to improve trial execution and efficiency.

🎯 Requirements

• Life Sciences, Medicine, Pharmacy, Nursing or related academic background, or equivalent experience.
• Minimum 4 years of site monitoring experience in global trials as Lead Monitor or equivalent.
• Strong knowledge of Canadian and US regulatory guidelines and clinical research practices.
• Experience overseeing Phase I–III monitoring activities; oncology experience preferred.
• Experience with advanced therapies (CAR-T, cell/gene therapy) is an asset; GI indications a plus.
• Excellent communication, collaboration, and problem-solving skills; English proficiency.

🎁 Benefits

• Career advancement within a growing global clinical research environment.
• Exposure to diverse therapeutic areas and international trials.
• Continuous learning and professional development support.
• Collaborative culture focused on quality and teamwork.
• Meaningful impact on medical research and patient outcomes.
• Significant ownership, responsibility, and career growth potential.