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

Role: Clinical Research Associate (CRA) responsible for site-level oversight of clinical trial quality, compliance, and data integrity across all trial phases. Objectives include ensuring adherence to protocols, GCP, SOPs, and regulatory standards; verifying data accuracy; and supporting site qualification, initiation, monitoring, and close-out activities. Responsibilities encompass building site relationships, training site staff, assessing investigator resources, supporting regulatory audits, managing site risk and performance metrics, and assisting with study drug oversight. Qualifications: Bachelor's degree in life sciences or related field; 2-3 years clinical research experience, preferably in pharma/biotech settings; proficiency in clinical systems (CTMS, eTMF, eDC, RBQM tools); knowledge of ICH/GCP guidelines, regulations, and clinical trial processes. Experience in drug development, with exposure to multiple therapeutic areas, is preferred. The role requires up to 70% travel and involves working across various medical settings, ensuring compliance, and supporting regulatory inspections. The position is field-based, supporting an investigational pipeline, with a focus on site monitoring, data quality, and regulatory adherence in a dynamic environment.