Clinical Research Support
Clinical Trial Contracting staff develop budgets and negotiate contracts related to clinical trials.
The Clinical Trials Office (CTO) provides support to Moffitt’s multidisciplinary clinical programs as well as the Moffitt Screening Center. The CTO employs research nurses, clinical trial coordinators, research data specialists and regulatory specialists to support clinical trials. The staff work together as a team to support physicians-scientists.
The Protocol Support Office (PSO) staff, consisting of protocol analysts and committee coordinators, serve to assist Moffitt investigators with efficient and accurate processing of research protocols, including Scientific Review, Review of Serious Adverse Events, Data and Safety Monitoring and administration of OnCore, Moffitt’s Clinical Trials Data Management system.
The Cancer Center’s culture and organizational structure underscore a basic value: collaboration and inter-disciplinary teamwork. The size of the Center, its singular focus on cancer and the close interaction and outreach with academic partners and caregivers throughout the state, nation and world, all contribute to the rich, collegial and collaborative environment required to perform outstanding cancer research.