Intramural Continuing Umbrella of Research Experiences (iCURE) Applications (NCI)

Forms and Documents

Forms and supporting documents for this ICR

Document	Type	Status	Availability
Form 4 Request for Reference iCURE Program	Form	Unchanged	Available
Form 1 iCURE Postdoc Application	Form	Modified	Available
Form 2 iCURE GradStudents Application	Form and Instruction	Modified	Available
Form 1 Screenshot iCURE Postbac Application	Form	Modified	Available
ChangeRequestMemo 10.28.2019 CRCHD iCURE (1).docx	Justification for No Material/Nonsubstantive Change	Uploaded 2019-11-01	Available
iCURE OMB Burden Statement (1).docx	Supplementary Document	Uploaded 2019-11-01	Available
iCure 30-day 2018-22319.pdf	Supplementary Document	Uploaded 2018-10-16	Available
Attach7_PIA-iCURE-HHS Approved.pdf	Supplementary Document	Uploaded 2018-10-16	Available
Attach5_PrivacyActMemo-NCI iCURE.pdf	Supplementary Document	Uploaded 2018-10-16	Available
SSA iCURE_Final_10-16.18.docx	Supporting Statement A	Uploaded 2018-10-16	Available

IC Document Collections

Information collection document groups

IC ID	Collection	Type	Status	Form
233551	Reference Letter	Form	Unchanged	Request for Reference iCURE Program
233550	Postdoctoral Fellowship Application	Form	Modified	iCURE Postdoc Application
233550	Postdoctoral Fellowship Application	Instruction	Modified
233549	Graduate Student Application	Form and Instruction	Modified	iCURE GradStudents Application
233549	Graduate Student Application	Instruction	Modified
233548	Postbac Supplemental Application	Form	Modified	Screenshot iCURE Postbac Application
233548	Postbac Supplemental Application	Instruction	Modified

ICR Details

OMB Control No: 0925-0758	ICR Reference No: 201911-0925-001
Status: Historical Active	Previous ICR Reference No: 201810-0925-004
Agency/Subagency: HHS/NIH	Agency Tracking No:
Title: Intramural Continuing Umbrella of Research Experiences (iCURE) Applications (NCI)
Type of Information Collection: No material or nonsubstantive change to a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Approved without change	Conclusion Date: 11/15/2019
Retrieve Notice of Action (NOA)	Date Received in OIRA: 11/04/2019
Terms of Clearance:

table that charts list comparision

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	11/30/2021	11/30/2021	11/30/2021
Responses	370	0	370
Time Burden (Hours)	238	0	305
Cost Burden (Dollars)	0	0	0

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Abstract: The new Intramural Continuing Umbrella of Research Experiences (iCURE) program supports mentored research experiences for qualified post-baccalaureate (including post masters) individuals, graduate students, and postdoctoral fellows in the multidisciplinary National Cancer Institute (NCI) intramural research environment.

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Authorizing Statute(s): US Code: 42 USC 285a-2(b)(3) Name of Law: Public Health Service Act
  

Citations for New Statutory Requirements: None

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Associated Rulemaking Information
RIN:	Stage of Rulemaking:	Federal Register Citation:	Date:
	Not associated with rulemaking

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Federal Register Notices & Comments
60-day Notice:	Federal Register Citation:	Citation Date:
	83 FR 35665	07/27/2018
30-day Notice:	Federal Register Citation:	Citation Date:
	83 FR 51965	10/15/2018
Did the Agency receive public comments on this ICR? No

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Number of Information Collection (IC) in this ICR: 4

table that charts list of burden

IC Title	Form No.	Form Name
Graduate Student Application	2	iCURE GradStudents Application
Postbac Supplemental Application	1	Screenshot iCURE Postbac Application
Postdoctoral Fellowship Application	1	iCURE Postdoc Application
Reference Letter	4	Request for Reference iCURE Program

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ICR Summary of Burden

table that charts list of burden

	Total Approved	Previously Approved	Change Due to New Statute	Change Due to Agency Discretion	Change Due to Adjustment in Estimate	Change Due to Potential Violation of the PRA
Annual Number of Responses	370	370	0	0	0	0
Annual Time Burden (Hours)	238	305	0	-67	0	0
Annual Cost Burden (Dollars)	0	0	0	0	0	0

Burden increases because of Program Change due to Agency Discretion: No

Burden Increase Due to:

Burden decreases because of Program Change due to Agency Discretion: Yes

Burden Reduction Due to: Miscellaneous Actions

Short Statement: As indicated in A.3 of the approved Supporting Statement A, an electronic application system was being designed. This system, the iCURE Management System (IMS), has been developed and is ready to launch. With this new use of Information Technology there is a reduction in both the Burden Hours and Respondent Cost.

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Annual Cost to Federal Government: $188,673

Does this IC contain surveys, censuses, or employ statistical methods? No

Does this ICR request any personally identifiable information (see OMB Circular No. A-130 for an explanation of this term)? Please consult with your agency's privacy program when making this determination.     Yes

Does this ICR include a form that requires a Privacy Act Statement (see 5 U.S.C. §552a(e)(3))? Please consult with your agency's privacy program when making this determination.     Yes

Is this ICR related to the Affordable Care Act [Pub. L. 111-148 & 111-152]? No

Is this ICR related to the Dodd-Frank Wall Street Reform and Consumer Protection Act, [Pub. L. 111-203]? No

Is this ICR related to the American Recovery and Reinvestment Act of 2009 (ARRA)? No

Is this ICR related to the Pandemic Response? Uncollected

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Common Form ICR:  No

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On behalf of this Federal agency, I certify that the collection of information encompassed by this request complies with 5 CFR 1320.9 and the related provisions of 5 CFR 1320.8(b)(3).

The following is a summary of the topics, regarding the proposed collection of information, that the certification covers:

(a) It is necessary for the proper performance of agency functions;

(b) It avoids unnecessary duplication;

(c) It reduces burden on small entities;

(d) It uses plain, coherent, and unambiguous language that is understandable to respondents;

(e) Its implementation will be consistent and compatible with current reporting and recordkeeping practices;

(f) It indicates the retention periods for recordkeeping requirements;

(g) It informs respondents of the information called for under 5 CFR 1320.8 (b)(3) about:

(i) Why the information is being collected;

(ii) Use of information;

(iii) Burden estimate;

(iv) Nature of response (voluntary, required for a benefit, or mandatory);

(v) Nature and extent of confidentiality; and

(vi) Need to display currently valid OMB control number;

(h) It was developed by an office that has planned and allocated resources for the efficient and effective management and use of the information to be collected.

(i) It uses effective and efficient statistical survey methodology (if applicable); and

(j) It makes appropriate use of information technology.

If you are unable to certify compliance with any of these provisions, identify the item by leaving the box unchecked and explain the reason in the Supporting Statement.

Certification Date: 11/04/2019

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