Training Requirements

All of our coordinators are licensed nurses with a minimum of 5 years experience in performing clinical trials, are certified by ACRP or CCRP and are all HAZMAT and IATA certified. They are required to attend the monthly GCP and SOP training offered at the center and must complete CME requirements for ongoing research and re-certification. All of our principle investigators are also certified by ACRP, certified by their medical specialty board, must attend the monthly GCP and Standard Operating Procedure training and must complete CME requirements for continued ACRP and medical board certification. All coordinators are experienced with IVRS systems (ICON, RAMOS) and EDC (Medidata, Inform, PDS).

Each month there are 3 mandatory weekly meetings of the research staff. One meeting focuses on recruitment and retention strategies for each trial along with reviewing all adverse events, IND safety reports and achieved metrics. The other meeting is an internal audit of research charts and regulatory binders for compliance with the protocol, SOPs and FDA, ICH-GCP guidelines. The third meeting is training on GCP and Paragon's SOPs.