DMASC

The Data Management, Auditing, and Statistical Center for the Cancer Prevention Clinical Trials Network (CP‑CTNet)

About CP-CTNet

The key components of CP-CTNet are the CP-CTNet sites and the CP-CTNet Data Management, Auditing, and Statistical Center (DMASC). Each CP-CTNet site consists of a Lead Academic Organization (LAO) and Affiliated Organizations (AOs) that work together to perform cancer prevention clinical trials.

About DMASC

The Data Management, Auditing, and Statistical Center coordinates cross-network activities for centralized data management and reporting, clinical trials auditing, statistics, and administrative coordination across CP-CTNet Sites. In addition, DMASC collaborates with, and advises, CP-CTNet Sites with respect to trial design and protocol development.

DMASC is led by Jens Eickhoff, PhD, of the University of Wisconsin (Multiple Principal Investigator) and Sue Siminski, MS, MBA, of Frontier Science Foundation (Multiple Principal Investigator).

DMASC

DCP

Lead Academic Organizations (LAOs)

Affiliated Organizations (AOs) – Active

Affiliated Organizations (AOs)

Data Management and Reporting

  • Centralized data collection system via Medidata Rave®
  • 24/7 user support
  • Written data management quality procedures
  • Site training, reporting of data and metrics

Clinical Trials Auditing

  • Independent auditing of trials and processes
  • Guidance to ensure GCP, regulatory, and NCI guidelines are followed
  • Collaboration with Site staff to identify systemic improvements

Administration and Coordination

  • Unified operational structure
  • Procedural documentation
  • Biospecimen inventory

Statistics

  • Statistical consultation and expertise for all CP-CTNet clinical trials
  • Primary statisticians of record for all cross-network clinical trials
  • Statistical support to CP-CTNet Sites