The CCR nursing team collaborates with multidisciplinary teams to ensure the completion of research objectives while maintaining safety, efficiency, and data integrity. Registered nurses assist in developing MD orders and data collection tools.
Our facilities are strategically located at the heart of the UCI Medical Center in Orange and the UCI School of Medicine campus in Irvine. These locations provide us with direct access to world-renowned scientists and state-of-the-art resources, facilitating groundbreaking research across a spectrum of diseases. Our clinics are equipped with routine and specialty equipment and interfaced with Electronic Health Records (EHR) to minimize data collection errors.
Our pre-award/start-up team assists with budget development, ensuring it reflects the trial’s cost and accounts for all necessary expenses. We also help negotiate with funding sources and oversee contracting, calendar creation, and coverage analysis.
Post-award team
The post-award team manages study funds and accounting for all expenses. We assist in creating accounts, managing budgets, tracking expenses, invoicing sponsors, and distributing funds.
Our Business Development team builds strategic alliances with sponsors, including pharmaceutical companies, medical device innovators, and CROs, to advance clinical research. Key areas of focus include:
Our Recruitment team provides enrollment support, including marketing, advertisement, and outreach initiatives, to achieve accrual goals. We develop tailored recruitment strategies in collaboration with sponsors to ensure timely trial completion.
The OnCore support team assists with the Clinical Trials Management System (CTMS), including support, training, system improvements and standardized operating procedures. The data and analytics team specializes in analyzing trial data, generating reports, managing electronic case report forms (eCRF) through REDCap and harmonizing data from various project sites.
Our Project Management team ensures successful, on-time and on-budget project execution by maintaining processes, standards and best practices, offering strategic advice and guidance throughout every stage of project implementation.
Contact Our Business Development Team
Thank you for your interest with our team.
One of our specialists will be in contact with you soon.
Privacy Policy
University of California, Irvine - Study Information Sheet
UCI Center for Clinical Research Potential Participant Database
Lead Researcher
Maheswari Senthil, MD
UCI Center for Clinical Research
In the instance of parental permission, “You” refers to “Your child.”
Please read the information below and ask questions about anything that you do not understand. A
researcher listed above will be available to answer your questions.
You are being asked to participate in a clinical research potential participant database to identify
potential clinical research studies you may be eligible for. Participation in this database is voluntary.
You may choose to skip any question. You may refuse to participate or discontinue your involvement
at any time without penalty or loss of benefits. You are free to withdraw from this database at any
time. If you decide to withdraw from this database you should notify the research team
immediately.
You are eligible to participate in this study if you may be interested in participating in a research trial
at UCI Health
We would like to interview you to learn more about your eligibility for current clinical research studies
at UCI. The interview will last about 5-30 minutes, depending on the extent of your medical history.
Possible risks/discomforts associated with the database are hearing about potential clinical research
studies that may not be of interest to you, invasion of your privacy, or a potential breach of
confidentiality.
There are no direct benefits from participation in the database. However, this database may help
inform you on clinical research studies that you may be eligible for. Participation in UCI clinical
research studies help us gain important data and knowledge that may lead to improved treatment
options for people with similar conditions to you in the future.
There are no alternative procedures available. The only alternative is not to participate in this study.
There is no compensation for your participation in this database.
There is no cost to you for participation in this database.
All information collected will be stored confidentially in a world-class securely-hosted application,
“RealTime CTMS,” with robust data protections and encryption. This application has HIPAA compliant
architecture and application rules to ensure data privacy and regulatory compliance.
Researchers will use your information to assess your eligibility for current and future clinical research
studies at UCI. You may opt out at any time.
The research team, authorized UCI personnel, and regulatory entities, may have access to your
study records to protect your safety and welfare.
While the research team will make every effort to keep your personal information confidential, it is
possible that an unauthorized person might see it. We cannot guarantee total privacy.
Future Research Use
Researchers will use your information to conduct this study. Once the study is done using your
information, we may share them with other researchers so they can use them for other studies in the
future. We will not share your name or any other private identifiable information that would let the
researchers know who you are. We will not ask you for additional permission to share this de-identified
information
Data Retention - In accordance with UC Office of the President policy, information will be retained for
10 years after the end of the calendar year in which the research is completed.
If, during the course of this study, significant new information becomes available that may relate to
your willingness to continue to participate, this information will be provided to you by the research
team listed at the top of the form.
If you have any comments, concerns, or questions regarding the conduct of this research please
contact the researchers listed at the top of this form
Please contact the UCI Institutional Review Board by phone, (949) 824-8170, by e-mail at
IRB@research.uci.edu or at 160 Aldrich Hall, Irvine, CA 92697-7600 if you are unable to reach the
researchers listed at the top of the form and have general questions; have concerns or complaints
about the research; have questions about your rights as a research subject; or have general
comments or suggestions.
What is an IRB? An Institutional Review Board (IRB) is a committee made up of scientists and nonscientists.
The IRB’s role is to protect the rights and welfare of human subjects involved in
research. The IRB also assures that the research complies with applicable regulations, laws, and
institutional policies.
UCI