Specialized Centers of Clinically Oriented
Research (SCCOR) Programs
National Heart, Lung, and Blood
Revised May 13, 2005
Q: Where can I read about the SCCOR
A. A description of the SCCOR program is available on the NHLBI Specialized Centers of Clinically Oriented Research (SCCOR) Program Description Page and guidance for preparing an application is on the NHLBI Special Instructions for Specialized Centers of Clinically Oriented Research (SCCOR) Grant Applications. NHLBI Links to current and future solicitations for SCCORs can be found on the NHLBI Grants and Contracts Page.
Q: What is a SCCOR?
A: A SCCOR is a
multi-project grant to enable multidisciplinary basic and clinical research
that is focused on clinically-relevant questions. The key new requirement in
the SCCOR is that at least one-half of funded projects must be clinical. As
always, there must be at least three fundable projects, the Principal
Investigator (PI) should be an established research scientist who will commit
at least 25% of his/her time to the SCCOR, and the PI must have a fundable
project. All proposed projects must be designed to be completed within the
five-year duration of a SCCOR award.
Q: Must an overall PI of a SCCOR be a
A: No. However, the PI should be experienced and
knowledgeable in clinical research, including human subject recruitment and all
rules and regulations governing the participation of human subjects in
Q: What is a clinical project?
clinical project is one in which the project investigators have direct contact
with patients having the disease or condition of interest. Normal healthy
subjects may be included, but only in combination with patients. In studies
involving the use of human specimens, the investigators must have direct
interaction with the patient from whom the specimen is obtained and relate the
research results to the patient status or outcome for this to be considered a
clinical project. It is intended that the requirement for investigator
interaction with the study participants will eliminate research involving
Q: An investigator can obtain samples from
patients enrolled in a clinical treatment trial being conducted by industry in
order to measure pathogenic markers that will be evaluated with respect to
individual patient outcome. Does this qualify as a clinical project?
No. If the investigators are not involved as a site in the clinical study, this
would not be considered a clinical project. The SCCOR investigators must
interact directly with the participants in a study.
Q: Can a project involving studies of non-human
primates and/or other animals AND patients qualify as a clinical
A: Yes, but the primary focus of the project must be
Q: Can an institution collaborate with other
institution(s) in order to obtain sufficient patients to perform meaningful
A: Yes; the usual subcontracting requirements
Q: Do indirect costs of institutions under a
subcontract count toward the $2.5 million direct cost cap?
Indirect costs for subcontracts are considered direct costs, but do not count
toward the direct cost cap.
Q: Can an investigator be the PI for more than two
A: Yes, but the investigator must devote the required effort
(20% for each project; 25% for the overall PI).
Q. What is a Skills Development Core?
This is a new optional Core to support activities to assist in the development
of the research skills of new clinical investigators. It provides up to
$100,000 in direct costs in addition to the cap.
Q: Do I have to apply for a Skills Development
Q: Will I be penalized if my application does not
include a Skills Development Core?
A: No, the priority score of the
Skills Development Core will not be entered into the calculation of the overall
SCCOR priority score.
Q: Can the leader of the Skills Development Core be
the SCCOR PI?
A: Yes, but the individual must devote 5% effort to the
Core as well as 25% effort as the PI of the SCCOR.
Q: Can my institution submit two applications for
the same SCCOR program?
A: Yes, but reviewers are likely to be
skeptical about the viability of two complete SCCORs from one institution,
especially with the increased requirement for clinically-oriented research.
Each application must have a different PI.
Q: Can an institution outside of the United States
A: No, but an individual project or parts of a project could be
from a non-US institution.
Q: Is a letter of intent required?
but it helps the Institute staff to plan the review. If you intend to submit an
application, check the information in the RFAs for the due dates and
Q: Can I personally deliver the application on the
due date at NIH?
A: No, NIH no longer accepts applications in person;
they must be either mailed or sent by one of the overnight delivery services.
Questions and Answers in This Section are Specific for the SCCOR RFAs Listed Below
- RFA-HL-05-009: SCCOR in Host Factors in Chronic Lung Diseases
- RFA-HL-05-008: SCCOR In Chronic Obstructive Pulmonary Disease (COPD)
- RFA-HL-05-007: SCCOR in Pulmonary Vascular Disease
Q: Are grants related to cystic fibrosis appropriate for the recent COPD SCCOR RFA, or should CF NOT be considered a chronic obstructive pulmonary disease in this context?
A: Cystic fibrosis is not considered a chronic obstructive pulmonary disease for the SCCOR program in COPD. Proposed work related to cystic fibrosis will not be responsive to this RFA.
Q: Are these initiatives open to non-USA centers?
A: These initiatives are not open to non-USA centers. Please refer to section 1-A and 3-4 of the RFAs.
Q: Can a Clinical Core contain pilot clinical studies?
A: No. The purpose of a Core is to provide services to two or more research projects. All research studies must be included in the projects.
Q: May one person apply as a collaborator/co-investigator on two independent SCCOR applications?
A: NHLBI has no problem with your agreeing to participate in both SCCOR programs as long as there is no administrative, scientific, or budgetary overlap and the projects are not interdependent.
Q: Can a SCCOR project contain both basic and clinical research?
A: The spirit and intent of the SCCOR, as you know, is that at least half of the funded research is clinical. Please be aware that if a program contains more basic than clinical research when it is received, it will be considered as being non-responsive. The announcement states that a single project may integrate basic and clinical research. Keep in mind, however, that to be counted as "clinical,” a project must be predominately clinical (i.e., a major portion of the work involves direct interaction with human subjects.)
Q: If I submit 2 projects that are mostly clinical research, but do contain some basic research, and one project that is all clinical research, how many basic research projects may I submit- two or three?
A: If you were to have 2 projects that are predominately clinical but also include basic research, plus one purely clinical project, we recommend that you plan for just 2 additional basic research projects, as opposed to 3. It would be very helpful to us if you would include in the application for each of the combined clinical/basic research projects your estimate of the percentage of the project that is clinical research.
Q: Can a basic scientist be the PI of a clinical project?
A: A clinical project may have a basic scientist as the PI and a clinician as Co-Investigator, e.g., this arrangement is appropriate for a project concerning the evaluation of noninvasive technology to detect pulmonary hypertension. Please note, however, that the announcement (Section III, 3. Other-Special Eligibility Criteria, Item 10) indicates that leaders of clinical projects should have experience in clinical research as defined above.
Q: What is the application receipt date?
A: Applications must be received on or before the receipt date of August 17, 2005.