Office of Clinical Research
Site Activation Turn Around Times | Target | Current |
---|---|---|
Cycle time from draft budget to final budget
|
10 days
|
14 days
|
Cycle time from feasibility assessment to fully executed contract
|
30 days
|
45 days
|
Cycle time from fully executed contract to first enrollment
|
14 days
|
21 days
|
Cycle time from IRB submission to IRB approval
|
14 days
|
30 days
|
Facility & Staffing | Target | Current |
---|---|---|
Average PI years of experience
|
15 Years
|
15 Years
|
Certified Clinical Research Coordinators
|
5
|
2
|
Average research staff level of proficiency in EDC, IVRS, EMR, and CTMS
|
High
|
Mod
|
Percentage of studies that have used local lab & imaging successfully
|
100%
|
100%
|
Clinical Trials Summary | Target | Current |
---|---|---|
Number of Active Trials
|
50
|
30
|
Number of Departments involved in Research
|
10
|
8
|
% of clinical trials that concluded with target patient accrual
|
85
|
52
|
Number of Enrollment/Randomizations
|
1242
|
656
|
- About 60 years of combined JPS PI research experience
- About 30 years combined coordinator experience
- Two ACRP certified research coordinators. Other coordinators eligible soon
- ACRP certified clinical research manager
- One Project Coordinator to interphase between clinical trials, data management and analytics
- A pharmacy team with many years of research drug experience
- One Sr. Business Intelligence Specialist to query EMR on potential patients for new studies
- Grants Management team to facilitate federal, state and other research grants
- Rapid access to Level I Trauma facility
- CAP and CLIA certified lab – Onsite
- Phlebotomy labs –
- Availability of phlebotomy labs for blood draw
- Five (5) phlebotomy certified coordinators
- Dedicated research processing space with centrifuges and more
- Imaging labs – Onsite CT scans, MRI, PET, bone scans and X-rays among others
- Exam rooms – Availability of exam rooms to ensure privacy
- Pharmacy – Research oriented pharmacist to help with compounding, infusions and other pharmacist related consults.
- Technology
- Software
- Clinical Trial Management System (CTMS) – Allegro
- UCM for contract management
- Complion an eRegulatory document management tool
- IRBnet for local IRB protocol submission and tracking
- CITI for GCP and Biomedical research training
- MedRegs
- Statistical software (R and more)
- High speed internet access
- Research adaptive EMR via EPIC
- Software
- Monitoring space for CRAs
- Equipment
- Defibrillators
- ECG Machines
- -20 degree freezer
- -80 degree freezer
- Back up generator
- 24HR call - coordinator managed
Geographic Area:
JPS has a well-defined catchment area that encompasses Tarrant County, Texas, which is part of the Dallas-Fort Worth metropolitan area. Tarrant County is the third largest County in Texas with a population of 2.1 million people and an overall poverty of 13.5% [19, 20]. Tarrant County had the fifth highest population growth nationally between 2010 and 2019 (U.S. Census, March 26, 2020). In addition, the Dallas-Fort Worth-Arlington metropolitan area had the highest growth among U.S. metropolitan areas between 2010 and 2019.
Population Served/Pre-existing Strain:
JPS is a safety-net health system and serves vulnerable populations with barriers to healthcare including individuals who are low-income, uninsured, underinsured, racial/ethnic minorities, homeless, and have chronic health conditions. JPS Health Network provided care during 1.5 million patient encounters for 214,832 patients last year, of whom:
- 68% of patients were aged 20 – 64 years.
- 55% of patients were female; 45% were male.
- 35% were Hispanic, 27% were non-Hispanic Black, 27% non-Hispanic White, 4% were Asian, and 7% were other racial/ethnic groups.
- 27% were uninsured; 18% qualified for the JPS financial assistance program; 36% were on Medicaid, Medicare, or other government program; and 19% had private insurance.
- JPS patients speak many languages, for which JPS has a Language Services department to provide interpreters.
AUDIT & MONITORING TEAM
The Research Integrity Team (RIT) within the Office of Clinical Research has been tasked with ensuring research compliance by continuous monitoring and routine or for-cause auditing activities. This extends to sponsored studies where high-quality consenting practices, timely documentation, complete regulatory submission or reporting and strict adherence to approved protocols are paramount.
- Grant management
- Identity funding opportunities
- Assist with grant writing, e.g. statistical analysis plan
- Power analysis/sample size determination
- PI-initiated clinical trials
- Statistical analysis plan
- Power analysis/sample size determination
- Randomization
- Analytic results
- Comprehensive statistical support
- Study design
- Protocol development
- Data extraction from electronic medical record
- Power analysis/sample size determination
- Data analysis (e.g. modelling, prediction, testing)
- Research dissemination
- Manuscript writing
- Poster creation
- Abstract development