Clinical Trials Operations and Informatics Branch (CTOIB)

CTEP's Clinical Trials Operations and Informatics Branch (CTOIB) improves protocol development and conduct functions through the use of several systems for efficient business practices, informatics tools as well as central review of clinical trials for human safety and protection and process evaluation methods.

The Branch includes the Protocol and Information Office (PIO), the CTEP Enterprise System (ESYS), the NCI Central Institutional Review Board (CIRB), the Cancer Trials Support Unit (CTSU) and a component that analyzes the operations of NCI clinical trial Networks by using process evaluation tools.

PIO supports CTEP by collecting, processing, tracking, and monitoring all protocol-related information between CTEP and its extramural collaborators as well as with other CTEP and NCI programs.

The purpose of PIO is to:

• Facilitate the development and conduct of quality clinical trials in the most efficient and expeditious manner possible
• Minimize the administrative burden related to clinical trial development, conduct, and management on CTEP staff and the extramural community
• Abstract protocol-related keywords and milestones into CTEP ESYS to assist with CTEP decision making
• Promote, inform, and educate all concerned parties regarding NCI programs, policies, and objectives related to clinical trial development, conduct, and management

CTEP ESYS is a 22-application system that allows CTEP, other NCI staff, and the extramural community to enter pertinent agent and protocol-related data for the development and implementation of Network clinical trials. This includes reporting information to the FDA, managing agent inventory and orders, registering investigators, supporting audit activities, reporting accrual data, entering adverse event information, and managing disease and agent portfolios.

The primary objectives of the CTEP ESYS are to:

• Capture data and translate it into a usable and streamlined format to address scientific, safety, regulatory, and administrative requirements of clinical trials
• Eliminate data redundancy throughout the oncology community through integrated data systems
• Improve communication between CTEP and its collaborators
• Assure the security and confidentiality of proprietary and patient information
• Support broad patient access to clinical trials
• Expedite the protocol development and review process within both clinical trial organizations and reviewing bodies

The CTSU, another component of the Branch, works in tandem with ESYS. CTSU simplifies admittance to NCI-funded clinical trials for qualified clinical sites and supports the conduct of those clinical trials. CTSU membership provides access to a wide range of assistance, including patient enrollment and data-collection services, for eligible investigators. The CTSU website also offers a listing of active CTSU-supported clinical trial protocols, displays accrual information, and provides links to study abstracts.

The NCI CIRB helps reduce the administrative burden on local IRBs and investigators while continuing a high level of protection for human research participants. CIRB, with one centralized review, enables investigators to enroll patients into Network trials significantly faster than when employing the traditional method of assessment, which requires trial investigators in each site to obtain approval from a local IRB.

CTOIB also supports some process evaluation and data-analysis efforts for the NCI clinical trial Network systems. This includes using surveys and marketing analyses for the development and application of systematic accrual practices to aid challenging trials and evaluation of NCI programs, including the CIRB.