Advance your career as a Senior Clinical Research Associate at ICON Strategic Solutions, where you’ll support complex clinical studies in a cooperative team workplace. At ICON, the largest FSP organization, your role involves independent monitoring of investigational sites through phases II-IV. You will prepare documentation for regulatory submissions and ensure adherence to ICH-GCP principles.

Your skills will help enhance training for fellow CRAs while contributing to global health advancements. Key Responsibilities:
Independent setup and monitoring of clinical trials
Complete submissions for ethics and regulatory approval
Manage study cost efficiency throughout the process
Review documentation for feasibility studies
Mentor and train junior Clinical Research Associates Requirements:
18+ months of phase I-III monitoring experience
Prior involvement in medium-sized studies
Familiarity with ICH-GCP guidelines
Robust ability to meet critical deadlines
60% travel availability with a valid driver’s license Join ICON to make a global impact on healthcare innovation and patient outcomes.

📌 Senior Clinical Research Associate Role Toronto
🏢 ICON Strategic Solutions
📍 Toronto