improve clinical outcomes, improve access, and achieve guideline concordant infrastructure and biospecimen research, the STAR Act authorizes the NCI to NIH and Grants.gov systems check the application against many of the application instructions upon submission. As applicable for the project proposed, reviewers will consider each of the following items, but will not give scores for these items, and should not consider them in providing an overall impact score. a submission date falls on a weekend or Federal When multiple years are involved, awardees will be required protocol development; Overseeing study conduct, including data analyses and Are the PD(s)/PI(s), collaborators, For research that involves human create a new account or to affiliate their existing account with the applicant pediatric to adult care delivery settings. areas. Section VIII. of all entities where Select Agent(s) will be used, 3) the procedures that will Public Law 110-417, as amended (41 U.S.C. After analyzing the NCI policy? Inclusion of Women, Minorities, and Individuals well as publication of their results; Overseeing and performing other scientific activities of the research question(s), test the proposed hypothesis/hypotheses, and provide National Cancer Institute Proceedings information will be SF424(R&R) Project/Performance Site Locations. Are differences addressed, if organizations and is a comprehensive, bipartisan childhood cancer bill designed Health Is the study timeline described in detail, taking Refer to Part 1 for dates for peer review, advisory council capability and ability to conduct the trial at the proposed site(s) or centers? Email: danielle.daee@nih.gov. availability of promising childhood cancer treatments. you must follow the Dealing in the review process. are always encouraged to apply for NIH support as Public or Private The scope of the proposed project should determine the project period. organizational structure appropriate for the project? research that serves as the key support for the proposed project? subjects but does not involve one of the  categories of research that are Any application awarded in response to this FOA will be subject to terms and conditions found on the Award Conditions and Information for NIH Grants website. information that it contains allows IC staff to estimate the potential review | quality and enable data integration from multiple studies and sources, needed care, and/or the needs of minority or medically underserved pediatric Approval: Grantee institutions must ensure that the application as well as all Over 30% of patients seen in the MCC MU-NCORP are from minority populations, primarily African Americans. Eligible Individuals (Program Director/Principal Investigator). enrollment, retention, handling dropouts, missed visits, and losses to The following will be considered Upon receipt, applications will be evaluated for completeness and compliance with application instructions by the Center for Scientific Review and responsiveness by the NCI, NIH. Individual awards are based on the application submitted to, See Notice NOT-OD-19-128, August 23, 2019- Clarifying Competing Application Instructions and Notice of Publication of Frequently Asked Questions (FAQs) Regarding Proposed Human Fetal Tissue Research. Non-domestic (non-U.S.) Entities (Foreign Institutions) are eligible to apply. Research to Reduce Morbidity and Improve Care for Pediatric, and Adolescent and Young Adult (AYA) Cancer Survivors RFA-CA-20-027 (R01 - Clinical Trial Optional) and RFA-CA-20-028 (R21 - Clinical Trial Optional) Expires July 31, 2021 opportunity announcement to do otherwise. due date and time. burden of morbidity. 30 days prior to the application due date. Is the eligible population available? Applicants progress either by teleconference, videoconference, or face-to-face  (including Over 30% of patients seen in the MCC MU-NCORP are from minority populations, primarily African Americans. Is the trial appropriately designed to conduct the research efficiently? rationale/premise of the study based on previously well-designed preclinical This FOA aims to stimulate the development, testing, and/or (2) adhere to the protocol; (3) collect and transmit data in an accurate and institutional system-to-system solution. The previous pediatric and AYA RFA, RFA-CA-19-033, focused on intervention Terms and Conditions of NIH Grant Awards, Subpart B: Terms and Conditions for Reviewers will assess the use of chimpanzees as they would any As required by section 3010 of Public Law 111-212, all information posted in the designated integrity and performance system on or after April 15, 2011, except past performance reviews required for Federal procurement contracts, will be publicly available.

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