Become a Clinical Research Monitoring Specialist with IQVIA, focusing on site performance and data integrity across studies. Your expertise will be essential in maintaining regulatory compliance.In this role, you'll conduct comprehensive site monitoring visits to support the execution and integrity of clinical studies. You will assist in designing recruitment strategies, evaluate site practices, and facilitate training to ensure adherence to protocols. Your insights will help enhance quality and escalate issues when necessary.Key Responsibilities:Perform regular monitoring visits as per regulatory standardsAssist in recruitment planning and managementProvide essential training on study protocolsMonitor site adherence to GCP and ICH guidelinesMaintain detailed documentation and follow-up reportsRequirements:Bachelor's Degree in a scientific disciplineCRA training or prior practical experience requiredUnderstanding of regulatory requirements such as GCPAdept in Microsoft Office toolsStrong organizational and interpersonal skillsLeverage your clinical research experience to advance the quality and success of trials at IQVIA.#J-18808-Ljbffr

📌 Clinical Research Monitoring Specialist (Kirkland)
🏢 IQVIA
📍 Kirkland