Enhance clinical research integrity as a proactive Clinical Research Associate. Drive compliance and data accuracy while fostering robust relationships with site teams in a flexible environment.In this essential role, you'll be responsible for performing comprehensive site management and monitoring tasks to guarantee adherence to clinical study protocols. Your focus will include evaluating site performance, ensuring informed consent processes are appropriately followed, and documenting key activities. Your impact is vital in maintaining the quality and integrity of clinical trials.Key Responsibilities:Conduct monitoring visits and site assessmentsEnsure proper documentation and tracking of trial activitiesCollaborate with site staff for compliance trainingMonitor investigational product handling and safetyPrepare for audits and support readiness initiativesRequirements:Bachelor's degree or equivalent in a related fieldUnderstanding of Good Clinical Practice regulationsStrong analytical and computer skillsExcellent interpersonal and communication abilitiesCapacity for travel up to 75%Leverage your expertise to maintain the highest standards of clinical research and compliance across trials.

📌 Clinical Research Associate Ensuring Quality Monitoring And Compliance (Toronto)
🏢 Syneos Health
📍 Toronto