Site Manager - With over a decade of experience in directly coordinating clinical trial studies across

multiple indications for prominent sponsor companies, our Site Manager is adept in utilizing all EDC

systems, IRB submissions and maintenance, patient site visit direction and meticulous source document

upkeep. Their broad expertise ensures a smooth and compliant trial execution.

Study Coordinator 1 - A former CRA with over 10 years of monitoring experience, this coordinator

leverages their extensive trial expertise to ensure strict adherence to protocol, ICH/GCP guidelines,

ALCOA principles, and local regulations.

Study Coordinator 2 - Bringing in approximately 15 years of clinical trial experience as a study coordinator

and project manager, our Study Coordinator has a robust clinical background enhanced by working at

prestigious institutions. Their prior roles have provided comprehensive experience in handling complex

protocols and managing high-demand clinical environments.

*2 Medical Assistants, a licensed Phlebotomist and a Pharmacist are available onsite as needed.