CRA II

Clinical Research Associate II responsible for coordinating and monitoring all aspects of clinical trials, performing remote or on-site visits to assess protocol and regulatory compliance, managing required documentation, and ensuring adherence to ICH-GCP guidelines and SOPs. Drive data integrity through SDR/SDV reviews, conduct site visits, manage investigator payments, and maintain audit readiness. Develop strong relationships with investigational sites, apply risk-based monitoring and root cause analysis to identify process improvements, and communicate findings clearly to the project team. Requires collaboration with sponsors, ability to travel frequently (60-80% for some roles), and a Bachelor's degree in life sciences or RN credentials with relevant experience or fellowship completion.