Senior Clinical Research Associate

The Senior Clinical Research Associate will conduct site monitoring responsibilities, provide oversight and leadership in clinical trial execution, and ensure compliance and quality. Responsibilities include guiding CRAs, reviewing monitoring reports, conducting site visits, coordinating with departments, assisting in the development of monitoring plans and training, managing study budgets, performing qualification, initiation, interim, and close-out visits, ensuring data integrity through source document review, verifying TMF documents, conducting investigational product accountability, reviewing regulatory binders, maintaining site contact, ensuring GCP compliance, facilitating adverse event reporting, resolving data queries, identifying site issues, preparing for audits, assisting with CRA training, and mentoring CRAs.