Advance your career as a Senior Clinical Research Associate at ICON Strategic Solutions, where you’ll support complex clinical studies in a collaborative 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 • Strong 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 (Winnipeg)
🏢 ICON Strategic Solutions
📍 Winnipeg
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