Clinical Trials Core
Medical Director: Jeff Michalski, MD
The Siteman Cancer Center Clinical Trials Core (CTC) promotes excellence in cancer research for human subjects and provides support to all investigators in the cancer center for clinical research activities. Comprehensive services are available through the CTC for all aspects of protocol development, regulatory submissions, study coordination and data management. For more information, please contact the appropriate individual.
Protocol Development staff provide expertise and research assistance in the following areas:
- Study design
- Protocol and consent form development and editing
- Preparation of all required submission documentation, including IRB and PRMC applications, supplemental documents, data collection / case report forms
- Submissions to the FDA (IND or IDE)
- Initial registration and regular maintenance of records with ClinicalTrials.gov and the NCI Clinical Trials Reporting Program (CTRP), including reporting of results
- Creation of research databases (including ClinPortal and REDCap)
- Initial submission services to all entities is available to all investigators preparing oncologic clinical trials at no charge
- Study maintenance tasks may be performed by Protocol Development or Regulatory personnel for a fee. Please contact Stephanie Myles at firstname.lastname@example.org
Regulatory Services include:
- Management of all regulatory affairs, from protocol submission and processing of protocol-related actions and documents to trial closeout as well as working with the Protocol Review and Monitoring Committee (PRMC), Quality Assurance and Safety Monitoring Committee (QASMC) and IRB
- Records, documentation and full copies of clinical trials managed by the CTC will be kept in electronic files
- Information is also available through the Siteman database, and additional copies will be distributed to relevant clinical personnel
- This service is available to all cancer center members for a fee. Please contact Chloe Fournier at email@example.com
Study Coordination staff members provide services in all aspects of trial conduct and data management, including but not limited to:
- Trial logistics assessment
- Eligibility verification
- Study coordination
- Data collection
- Record retention
- Data safety and monitoring reporting
- Audit and monitoring preparation
- Adverse event assessment and reporting
- And data summary completion for analysis
- In addition, the office assists investigators with budget and contract development and other study-related activities. These services are available to all cancer center members for a fee. Please contact Lindsey Brunt at firstname.lastname@example.org
PRICING: Please contact the core for current pricing of services offered.
LOCATION: Barnes-Jewish Hospital Center for Outpatient Health(BJHCOH), eighth floor
As of April 7, 2008, the NIH requires investigators with a publication using Siteman (or other NIH-funded) shared resources to submit (or have submitted for them) their final, peer reviewed manuscripts to PubMed Central(PMC) upon acceptance of publication, to be made publicly available within 12 months of publication. Many journals automatically submit these for authors, but Washington University also has assistance available through the Becker Medical Library. Please see http://publicaccess.nih.gov/FAQ.htm#b7 for more information.
DOCUMENT USAGE: If research supported by the Clinical Trials Core results in publication, please acknowledge this support by including the following in your publication(s): We would like to thank the Alvin J. Siteman Cancer Center at Washington University School of Medicine and Barnes-Jewish Hospital in St. Louis, Missouri, for the use of the Clinical Trials Core which provided __________ service. The Siteman Cancer Center is supported in part by NCI Cancer Center Support Grant #P30 CA91842.