Clinical research professional at Vanderbilt University Medical Center. Currently strengthening my MPH with a biostatistics certificate and learning softwares such as SAS and SPSS.With over 2 years of experience in the field, I possess a deep understanding of regulatory compliance, patient recruitment, EDC, EMR, and data management.My expertise includes:- Coordinating Phase I-IV clinical trials in Orthopaedics- Ensuring compliance with FDA regulations, GCP guidelines, and institutional policies- Building strong relationships with investigators, sponsors, and study participants- Managing study data, including data entry, query resolution, and quality control- Handling invoices from sponsors and ensuring patients are paid- Collaborating with cross-functional teams to achieve study milestones and goalsI am passionate about the work that I do and pride myself on my work ethic and being a sponge to new information.