Florian L. Adragna, M.Sc.

CRA & GCP Auditor - Berlin

I am a freelance Clinical Research Associate (CRA) specializing in oncology, vaccines, and pneumology, and I also offer services as a GCP Auditor.

In clinical studies, high-quality data is crucial. This relies on accurate verification and, more importantly, on the proper training and support of site staff.

As a CRA, I ensure the accuracy of collected data and help site staff maintain precise documentation according to Good Clinical Practices (GCP) and sponsor requirements.

In addition to my CRA work, I offer my services to Quality Assurance departments, assisting with GCP audits to ensure that clinical trials comply with regulatory standards, protocols, and GCP guidelines, safeguarding both scientific integrity and participant safety.

With a background in genetics and extensive experience with study drugs and medical devices, I am committed to supporting international collaboration and advancing medical knowledge while upholding the rights and safety of trial participants.