Clinical Research Associate, Sponsor Dedicated

The Clinical Research Associate supports sponsor-dedicated monitoring activities across multiple sites, ensuring protocol compliance, data integrity, and regulatory documentation in line with GCP and ICH standards. Responsibilities Conduct site monitoring visits, including initiation, ongoing, and close-out activities according to protocol and GCP guidelinesDevelop and monitor subject recruitment plans to achieve enrollment targetsProvide protocol training and maintain regular communication with sites to manage expectations and resolve issuesMonitor study data quality, protocol adherence, and regulatory compliance; escalate concerns as neededTrack study progress related to regulatory submissions, enrollment, CRF completion, and data queries Qualifications & Skills Bachelor’s degree in a scientific or healthcare discipline preferredMinimum of 2 years of independent on-site monitoring experience as a CRAStrong knowledge of GCP and ICH requirementsProficiency with EDC, CTMS, eTMF, IVRS/IWRS systemsAdvanced skills in Microsoft Office suiteExcellent written and verbal communication in EnglishStrong organizational, problem-solving, and time management skills