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.