Sara Madrigal
Clinical Research Coordinator I
SC CTSI Role
Sara will support, facilitate, and coordinate daily clinical trial activities. She plays a critical role in the ensuring the informed consent process is performed and documented in compliance with FDA, GCP, IRB, HIPAA, SOPs, sponsor and institutional regulations and policies.
Contact Information
Professional Background
Sara has over 13 years of experience as a Clinical Research Coordinator at the University of Southern California, where she has had the opportunity to support a variety of research projects within the medical field. Her work primarily involves managing clinical trials, ensuring compliance with research protocols, coordinating with multidisciplinary teams, and facilitating patient interactions to ensure their safety and comfort throughout the study process.
Interests
Her interest is hiking, exploring local trails. She also enjoys spending quality time with family and friends.