Join PSI as a Senior Clinical Research Associate to lead a agile research team in optimizing clinical trial management. Focus on compliance and ensure timelines are met.In this pivotal role at PSI, a leader in contract research, you will leverage your site monitoring experience in a collaborative environment. Your responsibilities will include coordinating the monitoring process, conducting training sessions, and managing data integrity at a regional level. Engage directly with site teams to promote best practices and ensure adherence to various therapeutic protocols.Key Responsibilities:Conduct site audits and manage site-specific trainingMonitor enrollment metrics and implement improvementsOversee project team communications and updatesLead project meetings focused on compliance and timeline objectivesManage CAPA development and implementation processesRequirements:At least 4 years' experience in clinical monitoringStrong familiarity with Oncology research and regulationsProven track record in managing clinical teamsProficient in MS Office and data management systemsWillingness to travel frequently for project needsShape the future of clinical trials with your expertise and leadership at PSI.#J-18808-Ljbffr

📌 Senior Clinical Research Associate Role (Toronto)
🏢 PSI CRO
📍 Toronto