Senior Clinical Research Associate

The Senior Clinical Research Associate will conduct site monitoring responsibilities for clinical trials, providing oversight, leadership, and guidance to ensure compliance and quality. Key duties include reviewing monitoring reports, conducting site visits, ensuring protocol adherence, managing study budgets for stand-alone projects, preparing monitoring visit reports, verifying data integrity, performing quality control of documents, conducting investigational product accountability, maintaining contact with study sites, facilitating adverse event reporting, resolving data queries, identifying site issues, assisting with audit preparation, and mentoring new CRAs.