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Schedule . 1. Introduction: Jane Reusch2. PCIR:Bob Eckel3. Regulatory:Angela Wishon4. Biostatistics: John Kittelson5. Break out sessions6. Summary of breakout and closing remarks. Colorado Clinical
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1. CCTSI Nuts and BoltsHow the CCTSI Can Accelerate Your Research
2. Schedule 1. Introduction: Jane Reusch
2. PCIR: Bob Eckel
3. Regulatory: Angela Wishon
4. Biostatistics: John Kittelson
5. Break out sessions
6. Summary of breakout and closing remarks
3. Colorado Clinical & Translational Sciences Institute (CCTSI) Introduction to the
Organization and Structure
4. CCTSI at University of Colorado
5. CCTSI Organizational Structure
6. CCTSI Academic Home
7. Discovery Translation Organization
8. Workshop
9. Education, Training, & Career Development (ETCD) Organization
10. Case #1 Jr. Faculty #1 has demonstrated that milk has the ability to cure lupus in mice. She would like to investigate this in humans. With her mentor, she has put together a set of specific aims and laid out a study design. Her mentor tells her to go to that new GCRC/CCTSI thing and get the project going. They have people there who can help you.
11. Questions for Case #1 Who are those people?
How do you find them?
How do you fill out the on-line application?
What is the difference between the SARC and the IRB?
Can you get someone to look over the application/project before you turn it in?
How do you get help with statistics?
Is there a course for this?
12. PCIR: Organizational Structure
13. New structure of the CTRCs (evolving see website)
Centralized administration established
Robert Eckel/Kristin Benn
Tom Campbell / Pat Kittleson Adult CTRC
Philip Zeitler/ Cindy Scott TCH CTRC
Liz Connick/Mary Dang-UCB CTRC
Donald Leong NJC CTRC
Nursing TBA (outpt Lefevre; inpt-Bilton)
Bionutrition Janine Higgins
Core Laboratories Bryan Haugen
Streamlined centralized support services
Centralized protocol submission process
CTRC units and staff
Bionutrition core
Extended communication and services via the Nutrition Resource
Core assay laboratories
Bryan Haugen oversees consolidated core laboratory activities
COMIRB approval only now possible
Equitable distribution of support
(up to 7,000 per protocol CTRC resources)
14. Design and implement the PCIR Central to support clinical and translational research for investigators
New local scientific review process.
New Scientific Advisory and Review Committees (SARC) established.
Adult Wendy Kohrt, Ph.D and James Maloney, M.D. appointed as new co-chairs.
Pediatrics Jeff Galinkin, M.D., Ph.D. and Paul Fennessey, Ph.D. retained as co-chairs.
Protocol review process
Expanded investigator support services the new CTO model
In consideration, nothing implemented secondary to budget
Integration with other institutional resources
In progress (today)
Matchmaker program
In progress
15. Case #2 Jr. Faculty #2 has just been recruited to UCD and is going to be part of an NIH multicenter trial to examine exercise and drug X on breast cancer. He needs to get all the regulatory paperwork set up in order to participate. As far as he can tell, hes done a million online courses already.
16. Questions for Case #2 How does he find out what coursework is needed?
Is there someone who can help with an IND?
How does he register with clintrials.gov?
Why is the consent form so complicated?
How does he set up the contracts with the drug manufacturer?
Is there a course for this?
17. Regulatory Knowledge and Support Core Angela R. Charboneau Wishon, J.D.
Assistant Vice Chancellor for Regulatory Compliance
Director, CCTSI Regulatory Knowledge and Support Core
18. Overall Goals for this Program/Core Provide academic medical researchers a resource to master the complexities of regulatory issues associated with translational research;
Enhance existing research support services by providing the infrastructure to efficiently manage the vast array of regulatory issues across the affiliated institutions within the region; and
Assure consistent standards of human protection within our affiliated institutions.
19. Specific Aims in CTSA Grant Provide centralized services that facilitate preparation and maintenance of regulatory and administrative requirements and streamline researchers interactions with regulatory agencies.
Provide centralized services that provide a clinical research quality assurance program.
Provide consultative expertise and serve as a regulatory resource for researchers.
Provide training and be a resource for education on regulatory topics.
20. Organizational Structure
21. Case #3 Jr. Faculty #3 is writing a grant proposal and has no clue where to start with the statistics section.
22. Questions for Case #3 How do you get help with a power analysis?
Why would he want a statistician involved in the study before he has data?
Does he just need statistical advice or does he need a statistician on the project?
Is there a course for this?
23. UCD Biostatistics and theBiostatistics, Epidemiology, and Research Design (BERD) Program of the CCTSI John Kittelson, PhD
Monday October 12th, 2009
24. Outline Overview of UCD Biostatistics
Department of Biostatistics and Informatics
Colorado Biostatistics Consortium (CBC)
Research Institute (Pediatrics)
Others
BERD program
Overview of infrastructure
Education program
Consultation/collaboration
Methods development
25. UCD Biostatistics Overview Department of Biostatistics and Informatics:
Research (biostatistics methods)
Teaching:
Biostatistics graduate program (PhD, MS)
Masters of Public Health
Clinical Sciences Program
26. UCD Biostatistics Overview Department of Biostatistics and Informatics:
Collaborations:
Cancer Center Pharmacy/pharmacology
CAIANH COHO
CHN BDC
CFAR Psychiatry
27. UCD Biostatistics Overview Colorado Biostatistics Consortium (CBC)
A unit within the Department of Biostatistics
Created to develop additional biostatistics resources and to prepare for CTSA application
Funded through SIRC proposal
10 biostatisticians (including 4 from Pediatrics)
28. UCD Biostatistics Overview Research Institute (Childrens & Pediatrics)
A unit within the Department of Pediatrics
Collaborator in the CBC
4 biostatisticians
Wide-ranging collaborations in pediatric research
29. UCD Biostatistics Overview Others
Department of Family Medicine
Department of Anesthesiology
Division of Health Care Policy & Research
30. Biostatistics, Epidemiology, and Research Design (BERD) Program:
A collaboration across 10 groups:
Biostatistics Dept. Epidemiology Dept.
Pediatrics Dept. COHO
School of Pharmacy College of Nursing
National Jewish CAIANH
CO Prevention Center Kaiser Permanente
BERD Program
31. Broad Objective: To build breadth and depth through collaboration
32. Broad Objective: To build breadth and depth through collaboration
33. Broad Objective: To build breadth and depth through collaboration
34. Broad Objective: To build breadth and depth through collaboration
35. Education Program
Biostatistics short courses for non-statisticians
Data analysis short course
Study design short course (in planning)
Education seminar series
(3-4pm last Monday of most months)
Continuing education for biostatisticians:
Pharmacokinetic methods short course
Workshop on non-inferiority trials
Clinical trial design short course
Note formal courses in Biostatistics Dept:
Bios 6601/6602: Biostatistics I/II (non-statisticians)
Bios 6611/6612: Applied biostatistics (statisticians)
Bios 6648: Clinical trials
36. Consultation/collaboration
BERD program supports:
CCTSI Trainees (e.g., K-12 awardees)
CCTSI pilot grant awardees
CCTSI-supported studies on the CTRC
[Note: limitations apply]
Process:
Register your project at http://cbc.uchsc.edu
Statisticians meet weekly to review new work
37. New methods in translational statistics:
To advance the methodological aspects of translational research through original biostatistical methods research (including novel study design methods).
38. Recap of breakout results
Closing