
Healthcare and research professional with hands-on involvement in clinical trial workflows, study visit support, specimen collection, IATA-compliant specimen shipping, EDC data review, query resolution, protocol compliance, participant recruitment, informed consent, and regulatory documentation. Currently completing an MPH while supporting clinical research activities in a urology research department and performing delegated responsibilities on an industry-sponsored Phase III clinical trial. Brings a strong blend of clinical experience, research methodology, and public health training to clinical research coordination roles.