Sara Madrigal
Clinical Research Coordinator, Clinical Research Services
SC CTSI Role
Sara supports, facilitate, and coordinate 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 extensive experience as a Clinical Research Coordinator at the University of Southern California, where she has supported 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
Sara's interests are hiking, exploring local trails. She also enjoys spending quality time with family and friends.