Estee Garcia

Experienced coordinator who has conducted multiple studies such as NASH/MASH, VACCINES, DIABETES MELLITUS AND OBESITY.  I am CPT 1 certified with the State of California and am bilingual. English/Spanish

Responsible for the day-to-day management and execution of clinical trials, ensuring the study adheres to protocols, regulatory guidelines, and ethical standards by recruiting participants, collecting data, monitoring participant safety, and maintaining accurate records throughout the research process, acting as the primary point of contact for study participants and coordinating with the research team to successfully complete the study . Monitor participants for any adverse events, report them to the study team and regulatory authorities as required, and take appropriate actions to manage safety concerns. 
Ensure all study procedures are followed as per the protocol, including proper documentation and compliance with Good Clinical Practice (GCP) guidelines. 
Regularly communicate with the Principal Investigator (PI) on study progress, including any issues or concerns that arise, and prepare reports as needed. 

 

High school diploma/CPT 1 Certified