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The Office of Clinical and Translational Research (OCTR) was developed in response to a growing need for a centralized approach to the administration of clinical trials at the University
of Connecticut Health Center. Investigators can select services as their needs dictate, and our staff can answer questions regarding clinical trial agreements, clinical trial budgets,
and research financial compliance. Clinical trials contracts with industry are negotiated exclusively through this office. It is a “win-win-win” relationship for administrators,
investigators, and sponsors. Administration and Services
The Office of Clinical and Translational Research provides more than contract and budget negotiation. Our office also provides services related to retrospective information on patient
enrollment and the status of clinical trials in progress at the institution. Additionally, staff in OCTR will register investigator initiated studies on
clinicaltrials.gov to meet
publication prerequisites required by journals and mandated by FDA Amendments Act of 2007.
Research Financial Compliance and Monitoring
Staff in the OCTR will monitor the financial component of clinical trials to confirm that we are meeting institutional, as well as state and federal regulations. Research Financial
Compliance auditing, monitoring and close-out of FRS accounts are all pieces of the continuous monitoring process for all clinical trials which are being done at the University of
Connecticut Health Center.
Questions
If you have any questions regarding the services provided by the staff in the OCTR or you would like to set up an appointment to discuss services, please call us at 860-679-7816.
News Notes
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Per
Dr. Peter
Albersten, Associate Dean of Clinical Research Planning
and Coordination, effective September 1, 2009, all standard UMG and
JDH charges will be discounted 45% for Investigator
Initiated studies. For further information or
clarification, please contact Judy Kulakofsky at 860-679-7816.
News Notes will provide monthly research financial
compliance updates that are of importance to research
teams. Changes to policies, procedures and forms; as
well as information regarding educational sessions can
be found here.
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Revised 9/16/09 |
The Guide
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 The
Guide to Financial Compliance in Human Subjects Research has been compiled to assist the PI and the research team negotiate the increasingly complex world of research
financial compliance.
Requires Acrobat Reader |
Staff
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- Peter Albertsen, M.D.
Associate Dean
Clinical Research Planning and Coordination
- Judi Kulko, M.S.N., M.S.
Executive Administrator
Phone: 860-679-1395
Fax: 860-679-1856
Email: kulko@uchc.edu
- Judi Gilson
Coordinator
Pharmaceutical Contracts
Phone: 860-679-2742
Fax: 860-679-1856
Email: gilson@adp.uchc.edu
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- Judy Kulakofsky
Coordinator
Budgets and Budget Workbook
Phone: 860-679-7816
Fax: 860-679-1856
Email: kulakofsky@uchc.edu
- Judie Fine
Coordinator
Standard Operating Procedures
Clinical Trials Registration and Program Manual
Phone: 860-679-3366
Fax: 860-679-1318
Email: fine@nso.uchc.edu
- Clint Propfe
Reimbursement Analyst
Phone: 860-679-4369
Fax: 860-679-1856
Email:
propfe@uchc.edu
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