Elevate your clinical research career as a Clinical Research Associate! Manage and monitor studies in phases II and III while ensuring compliance and integrity throughout the study lifecycle.In this pivotal role, you'll focus on overseeing clinical studies, maintaining adherence to GCP, and building robust relationships with investigators. Your responsibilities will include the qualification and initiation of study sites, alongside supervising the study conduct to ensure regulatory compliance. Your role is vital to the success of clinical research initiatives.Key Responsibilities:Oversee monitoring of clinical studies in phases II-IIIEnsure compliance with Positive Clinical PracticesIdentify and initiate investigators and their sitesSupervise study conduct in line with regulationsManage adherence to study procedures and integrityRequirements:Bachelor's degree in life sciencesMinimum 1 year of CRA experience in relevant settingsExperienced in site initiation and close-out processesClinical study experience in phases II-IIIExcellent English communication proficiencyBring your expertise in monitoring and compliance to advance clinical research and support innovative treatments.

📌 Clinical Research Associate For Regulatory Compliant Trials (Ottawa)
🏢 Resourcing Life Science
📍 Ottawa