Clinical Research Associate- San Antonio / South-Central Texas Region

Role: Clinical Research Associate (CRA) overseeing site management and compliance for clinical trials at Bristol Myers Squibb. Responsibilities: conduct site qualification, initiation, monitoring, and close-out visits across all trial phases; verify data integrity and adherence to ICH GCP and local regulations; build relationships with internal teams, external sites, and vendors; support site qualification, performance assessment, and risk mitigation; prepare reports, support regulatory audits, and assist with start-up activities. Requirements: Bachelor’s degree in life sciences or related field; 2-3 years of clinical research experience, preferably in pharma/biotech settings; proficiency in clinical systems (CTMS, eTMF, RBQM tools); knowledge of ICH/GCP guidelines, clinical trial processes, and regulatory compliance; strong communication, organization, and analytical skills. Preferred: experience with remote and risk-based monitoring approaches, ability to work independently, and up to 70% travel. HighValue: site management across all phases, emphasis on data quality and compliance, extensive use of clinical system platforms, and involvement in regulatory audits. WorkSetup: field-based role in South-Central Texas, with significant travel.