• Deliver instructional lessons across various subjects and grade levels • Manage classroom behavior and maintain a positive learning environment• Monitor and assess student performance, providing feedback and support as needed• Implement engaging activities to reinforce learning objectives and promote student participation

• Managed participant enrollment, protocol adherence, and regulatory compliance for 15+ active clinical trials• Reorganized the master clinical trial file, improving documentation accuracy and easy access to available trials• Led weekly team meetings with investigators and study staff to discuss trial progress, troubleshoot issues, and ensure protocol compliance• Responsible for all IRB submissions, including new project applications, amendments, adverse events, and continuing reviews• Oversaw patient registration and data collection in OnCore (eCTMS) and external sponsor EDC systems• Trained and supervised 3 clinical research coordinators, providing mentorship and ongoing support

• Managed clinical trials and observational studies, ensuring adherence to IRB and GCP guidelines• Developed organizational tools, including training and manuals of operations and project timelines, to support study progress• Reviewed trial database regularly for adverse events and missing data; created action plans and contacted investigators and staff from multiple sites• Led weekly research team meetings with investigators and research staff to discuss study progress, prepared detailed agendas, and created and distributed minutes• Prepared and managed IRB and regulatory files, including consent forms, amendments, and continuing reviews and DSMB reports• Created and maintained 2 REDCap databases and surveys, ensuring accurate and timely data collection• Conducted remote and in-person clinical trial monitoring at multiple sites, ensuring regulatory compliance and data quality

• Managed all aspects of 3 trials (interventional clinical trial, observational study, and qualitative study), from start-up to maintenance, ensuring protocol adherence and participant recruitment• Collaborated with community health centers, conducted 25 qualitative interviews, and ensured protocol fidelity• Created multiple databases in REDCap for data tracking and analysis, ensuring data integrity and facilitating collaboration with statisticians• Designed study materials, including eCRFs and manual of operations, to ensure accurate data collection• Managed 3 study staff and conducted performance evaluations

• Managed a portfolio of pediatric and adult research projects involving cancer care, bioethics, adverse event reporting, return of genetic results, and knowledge of clinical trials from study inception to completion• Developed study protocols, consent forms, and case report forms for various research projects• Acted as a resource regarding IRB policies, general research practices, and database design for 3 fellows• Created multiple study databases in REDCap and Access and analyzed data for presentations and publications using Stata• Organized and led a monthly discussion group for 8-12 research assistants and coordinated faculty speakers and topics• Trained, supervised, and mentored 2 research assistants and conducted performance evaluations.