Clinical Trial Associate II

The Clinical Trial Associate II will provide support to the Director of Clinical Operations in the conduct of trials and may be responsible for managing startup activities, vendor communication, internal meetings or other project activities, as assigned. They will perform work within established protocols under general supervision, established processes, and regulations. Responsibilities include assisting with preparation of external and internal documentation, aiding Clinical Trial Manager(s) in site management, developing and updating clinical trial tracking tools, maintaining documentation accuracy, ensuring compliance with protocols, organizing study files, and tracking supply delivery.