Teams at Urology San Antonio

Designs and delivers training and competency programs for CMAs, LVNs, and reception staff across clinics. Coordinates new-hire onboarding, conducts skills validations, monitors training outcomes, ensures regulatory compliance, and partners with clinic leaders to close performance gaps and support workflow improvements.

Manages clinical research staff and study operations across multiple clinical trials. Oversees protocol compliance, participant visits, recruitment, data integrity, quality control, regulatory requirements, monitoring visits, sponsor communication, staff training, and enrollment performance. Supervises coordinators, recruiters, laboratory technicians, and data coordinators while supporting investigators and ensuring accurate, timely study documentation.

Coordinate and manage all aspects of prostate and bladder oncology clinical studies including screening, recruitment, data and specimen collection, database creation/maintenance, regulatory documentation, scheduling, and communication with investigators and sponsors. Support multiple concurrent studies, assist with protocol renewals/modifications, and ensure compliance with FDA/GCP and institutional policies.