The CRA II is a seasoned, experienced professional in monitoring and site management. Responsibilities will be dependent upon the type and timing of the program to which the CRA II is assigned and typically include activities involving start-up and study implementation, on-site monitoring of clinical research studies as well as on-going site management. Incumbents work independently as a study team member.

This contract position ensures that data collected for clinical studies is accurate, plausible, and traceable to source documentation, assisting in site management, and clinical study materials development.

Oversee multiple oncology trials, ensuring high-quality execution. Provide leadership and mentorship to junior flex team members. Act as Lead SM, training and guiding other Site Managers on study protocols. Develop essential study start-up documents, including SIV agendas. Represent Site Managers and Lead Trial Managers (LTMs) in key meetings.