Overview: The Sr. Clinical Trial Associate (CTA) will be responsible for providing Clinical Team members... activities, assisting with Trial Master File (TMF) documentation, and performing other administrative tasks. In addition, the Sr...
in life sciences or related discipline. 6+ years experience as a Clinical Research Associate. Extensive knowledge of trial...The Sr. CRA will be responsible for monitoring clinical studies at the site level, ensuring adherence to protocols...
Overview: The Sr CRA will be responsible for monitoring clinical studies at the site level ensuring adherence...-monitor with CRO or contracted CRAs. Supports the maintenance of documentation to clinical systems (Clinical Trial Management...