I apply my 2+ years of clinical research experience and my GCP and Medidata certifications to ensure the accuracy, completeness, and compliance of data collection and reporting for oncology trials. I collaborate with investigators, sponsors, and monitors to facilitate UAT Testing, eCRFs, data queries, audits, and submissions, and to provide training and support to site staff and patients.My passion for clinical research stems from my academic background in psychology and my interest in advancing the scientific knowledge and treatment of various health conditions. I have developed strong communication and study coordination skills through my previous roles as a Clinical Data Analyst, a Clinical Research Trainee, and a Research Data Coordinator, where I contributed to multiple projects involving data analysis, quality control, protocol adherence, and documentation. I enjoy being a leader and helping others around me grow, and I look forward to networking and meeting new professionals in the field.