Senior Clinical Research Associate

The Senior Clinical Research Associate will conduct site monitoring responsibilities for clinical trials, providing oversight and guidance to ensure compliance and quality. Responsibilities include reviewing monitoring visit reports, ensuring investigator site visits are appropriate and timely, assisting in the development of monitoring plans and training presentations, performing qualification, initiation, interim, and close-out visits, and ensuring data integrity through source document review. The role also involves investigational product accountability, regulatory binder review, maintaining contact with study sites, facilitating adverse event reporting, resolving data queries, identifying site issues, and assisting with CRA training and mentoring.