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.

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.

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.Description text goes here.

a licensed Phlebotomist and a Pharmacist are available onsite as needed.