Clinical Research Associate, Sponsor Dedicated

Clinical Research Associate role supporting sponsor-dedicated monitoring activities across multiple U.S. sites. Responsible for site management, protocol compliance, data integrity oversight, and regulatory documentation in accordance with GCP and ICH guidelines.

Responsibilities Conduct site monitoring visits including initiation, ongoing monitoring, and close-out activities per protocol and GCP Develop and track subject recruitment plans with sites to meet enrollment targets Deliver protocol training and maintain regular site communication to manage expectations and resolve issues Monitor study data quality, protocol adherence, and regulatory compliance; escalate concerns as needed Track study progress including regulatory submissions, enrollment, CRF completion, and data queries Requirements Bachelor's degree in scientific or healthcare discipline preferred At least 2 years independent on-site monitoring experience as CRA Strong knowledge of GCP and ICH regulatory requirements Proficiency with EDC, CTMS, eTMF, IVRS/IWRS systems Advanced Microsoft Office skills (Word, Excel, PowerPoint) Excellent written and verbal English communication abilities Strong organizational, problem-solving, and time management skills Compensation:

$74,500–$197,500 base (annualized)