This presentation will detail the importance of transparency, positivity, and professionalism framing all aspects of the process for evaluating the performance of clinical research associates (CRAs) during study site monitoring visits. It will review best preparation and communication practices for visit execution that will elevate the evaluation beyond a simple "pass or fail" determination, leading to a better understanding of competent performance, training needs, and the value of trust between evaluators and CRAs.
CEU: 1.00 ACRP
Speaker:
Elizabeth Weeks-Rowe, LVN, CCRA, Independent Clinical Research Consultant, Elizabeth Weeks-Rowe Consulting, LLC
Related Blog Content:
Who Monitors the Monitors? CRA Evaluations Essential to Better Trials and Relationships
Watch a Sneak Peek into the Session Content: