|
Welcome to the Clinical Trials Office at Rush University
Medical Center. Our mission is to facilitate the timely execution and
completion of high-quality clinical research at Rush. The Rush Clinical
Trials Office (CTO) offers a menu of services to assist Rush investigators
and industry sponsors with all aspects of clinical research. The CTO staff
has extensive training to ensure that studies are conducted in accordance
with sponsors¹ standards as well as with federal regulations and current
guidelines for good clinical practice.
Our services include facilitating timely:
- Identification of investigators
- Completion of regulatory documents
- Budgeting and contract negotiation
- IRB application submission
- Study initiation, patient recruitment and follow-up
- Study coordinator support
- Ongoing quality control monitoring
For more information, contact:
Rush Clinical Trials Office
1725 W. Harrison, Suite 439
Chicago, IL 60612
Fax: (312) 563-2734
Lisa Pitler, RN,MS,JD
Senior Director
Clinical Trials Processing Office
Michelle D. Hollins, BBA
Research Budget Administrator
(312) 563-2710
Lisa Pearsall
Recruitment and Marketing Coordinator
(312) 563-2712
Dr. Nahla Hasabou, FMG
Research Coordinator
(312) 942-3027
Sandra Mata
Administrative Assistant
(312) 563-2721
|