Clinical Trials Core
Medical Director: Jeff Michalski, MD
- Nick Fisher, MBA, Director of Operations, Clinical Research
Phone 314-747-5401, email@example.com
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
- Internal Education and Training
The Siteman Cancer Center Clinical Trials Core Education Program conducts a variety of educational sessions for new hires and established staff. Initially all new hires (in all job positions) receive the basic New Hire Orientation which consists of 3 sessions that are 3 hours each. Topics range from performance expectations, to protocol interpretation, informed consent process, research ethics and data integrity. Within a month, these sessions are followed by educational sessions targeting specific job roles and responsibilities (clinical, data, etc.). A comprehensive exam is completed by new staff pre and post orientation and again at 5 months to measure effectiveness of the education program. All staff are required to attend annual refreshers on informed consent and eligibility and whenever an event triggers an educational opportunity. These sessions are in addition to mandatory university requirements such as CITI and HIPAA training.
- Education for External Sites
The Siteman Cancer Center Clinical Trials Core Education Program also offers an 8 hour educational opportunity for external sites interested in general education for oncology clinical research. Topics include an overview of clinical research, research ethics, protocol interpretation, eligibility, informed consent process, data management, review of common lab values and interpretation, chemotherapy orders, Common Terminology Criteria for Adverse Events (CTCAE) and reportable events. This general education is followed by a “real world” shadowing session with role playing, form completion and a tour of the clinical research facilities.
- For more information please contact Amanda DeMoss at email@example.com.
PRICING: Please contact the core for current pricing of services offered.
LOCATION: Barnes-Jewish Hospital Center for Outpatient Health(BJHCOH), eighth floor