Advance your career as a Senior Clinical Research Associate at ICON Strategic Solutions, where you’ll support complex clinical studies in a collaborative team environment. 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