Advance your career as a Senior Clinical Research Associate at ICON Strategic Solutions, where you’ll support complex clinical studies in a collaborative team setting.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 AssociatesRequirements:- 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 licenseJoin ICON to make a global impact on healthcare innovation and patient outcomes.#J-18808-Ljbffr

📌 Clinical Monitoring Associate Ii Premier Research (Winnipeg)
🏢 Bilinguallink
📍 Winnipeg