Responsible for providing day-to-day supervision of the clinical research staff and operations assigned with oversight from responsible cto managers. Experience in the recruiting, training, development, and performance management of assigned staff. Supervision of daily operations includes study startup, trial coordination, and quality assurance needs. Time spent working with CTO manager to improve organizational performance through recommending areas or approaches for improvement activities, performing new procedures, collecting data and providing input to department discussions.

Responsible for maintaining sound conduct of Phase 1/2/3 clinical trials including, but not limited to recruitment, screening, education, enrollment, treatment and follow-up of eligible subjects according to protocol requirements. Assisted in initiating study treatment related patient education per protocol, and ensuring timely source documentation of protocol standards to facilitate data collection in various disease program departments. Experience in GI Oncology, Radiation Oncology, Immune Cell Therapies, Genitourinary Oncology, Thoracic Oncology, Gynecological Oncology, and Breast Oncology

Responsible for entering data pertaining to clinical trials. Assisted in various Clinical Trial departments at Moffitt Cancer Center. Worked with clinical trial coordinators, treating physicians, and clinical research associates to ensure quality data entry

Assist patients on a day-to-day basis in various outpatient clinics within the institute including Clinical Research Unit. Includes registering/scheduling orders and appointments requested by providers and associated clinical research coordinators as well as managing daily clinic flow. Related experience with Soarian Financials & Cerner Capstone application

Duty serving as voting member and primary or secondary reviewer at USF IRB meetings for initial, ongoing, and expedited review human study submissions. Responsible for considering the adequacy/ethical basis of inclusion/exclusion criteria in patient enrollment, methods of subject accrual, methods of data collection, and overall risk to subjects. Review of informed consent form adequacy, clarity, and appropriateness of information as well as risks/benefits to ensure informed subject participation. Duties carried out are done in accordance with University policy and applicable federal, state, and local laws as a non-scientific community member emphasizing patient advocacy

Data abstraction in various oncology disease sites including, but not limited to: Hematology Oncology, Gynecological Oncology, Neuro-Oncology, Thoracic Oncology, Radiation oncology, and Gastrointestinal Oncology, and Biomarker collection. Completed using Flatiron Health proprietary software and databases