Proposed Collection; 60-Day Comment Request; Center for Cancer Training (CCT) Application Form for Electronic Individual Development Plan (eIDP) (National Cancer Institute), 9537-9538 [2019-04856]
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Federal Register / Vol. 84, No. 51 / Friday, March 15, 2019 / Notices
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Dated: March 12, 2019.
Ronald J. Livingston, Jr.,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2019–04855 Filed 3–14–19; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Proposed Collection; 60-Day Comment
Request; Center for Cancer Training
(CCT) Application Form for Electronic
Individual Development Plan (eIDP)
(National Cancer Institute)
AGENCY:
National Institutes of Health,
HHS.
ACTION:
Notice.
In compliance with the
requirement of the Paperwork
SUMMARY:
collection techniques or other forms of
information technology.
Proposed Collection Title: Center for
Cancer Training (CCT) Application
Form for electronic Individual
Development Plan (eIDP), 0925–XXXX,
Exp., Date XX/XXXX, NEW, National
Cancer Institute (NCI), National
Institutes of Health (NIH).
Need and Use of Information
Collection: This information collection
request is to approve the electronic
Individual Development Plan (eIDP) for
three years. The National Cancer
Institute’s (NCI) Center for Cancer
Training (CCT) supports NCI’s goal of
training cancer researchers with various
educational levels (postbaccalaureate,
graduate students, postdoctoral fellows)
and for varying periods of time (3
months to 5 years). The eIDP is an
online, detailed questionnaire focused
on responses to career and professional
goals and expectations while the trainee
works at the NCI. The eIDP ensures the
NCI trainees are receiving proper career
and professional guidance, making
appropriate progress, and determining
activities to achieve their goals. The
eIDP is also used to track trainees’
career and professional goals and to
ensure trainees receive the tools needed
to achieve those goals. It is expected the
trainees will complete the eIDP
annually and that the eIDP process
could be improved by their responses.
The effectiveness of training could also
be enhanced by the reports received by
the trainees completing the eIDP.
Individual Development Plans have
been collected by paper and pencil from
trainees since 2001. With the
implementation of the electronic
system, a pilot of the eIDP was approved
by OMB (#0925–0046) and implemented
in December 2018. The pilot improved
the clarity of the instructions for the
eIDP system, and incorporated feedback
from the trainees to improve the overall
trainee IDP experience, which advances
the effectiveness of training.
OMB approval is requested for 3
years. There are no costs to respondents
other than their time. The total
estimated annualized burden are 1,209
hours.
Reduction Act of 1995 to provide
opportunity for public comment on
proposed data collection projects, the
National Institutes of Health, National
Cancer Institute (NCI) will publish
periodic summaries of propose projects
to be submitted to the Office of
Management and Budget (OMB) for
review and approval.
Comments regarding this
information collection are best assured
of having their full effect if received
within 60 days of the date of this
publication.
DATES:
To
obtain a copy of the data collection
plans and instruments, submit
comments in writing, or request more
information on the proposed project,
contact: Erika Ginsburg, Scientific
Program Analyst, Center for Cancer
Training, National Cancer Institute,
9609 Medical Center Drive, Room 2W–
106, Bethesda, Maryland, 20892 or call
non-toll-free number (240) 276–5627 or
Email your request, including your
address to: ginsbure@mail.nih.gov.
Formal requests for additional plans and
instruments must be requested in
writing.
FOR FURTHER INFORMATION CONTACT:
Section
3506(c)(2)(A) of the Paperwork
Reduction Act of 1995 requires: Written
comments and/or suggestions from the
public and affected agencies are invited
to address one or more of the following
points: (1) Whether the proposed
collection of information is necessary
for the proper performance of the
function of the agency, including
whether the information will have
practical utility; (2) The accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used; (3)
Ways to enhance the quality, utility, and
clarity of the information to be
collected; and (4) Ways to minimizes
the burden of the collection of
information on those who are to
respond, including the use of
appropriate automated, electronic,
mechanical, or other technological
SUPPLEMENTARY INFORMATION:
ESTIMATED ANNUALIZED BURDEN HOURS
amozie on DSK9F9SC42PROD with NOTICES
Type of
respondents
Number of
respondents
Number of
responses per
respondent
Average time
per response
(in hours)
Total annual
burden hours
Individuals—Trainees ......................................................................................
Individuals—Alumni .........................................................................................
Individuals—Feedback .....................................................................................
1,000
500
500
1
1
1
1
5/60
20/60
1,000
42
167
Total ..........................................................................................................
1,000
1,000
........................
1,209
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9538
Federal Register / Vol. 84, No. 51 / Friday, March 15, 2019 / Notices
Patricia M. Busche,
Project Clearance Liaison, National Cancer
Institute, National Institutes of Health.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
[FR Doc. 2019–04856 Filed 3–14–19; 8:45 am]
National Institutes of Health
BILLING CODE 4140–01–P
Center for Scientific Review; Notice of
Closed Meetings
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Institute on Alcohol Abuse
and Alcoholism; Notice of Closed
Meeting
amozie on DSK9F9SC42PROD with NOTICES
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended, notice is hereby given of the
following meeting.
The meeting will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended. The grant applications and
the discussions could disclose
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning
individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
Name of Committee: National Institute on
Alcohol Abuse and Alcoholism Special
Emphasis Panel; RFA–AA–19–001 Limited
Competition: Collaborative Study on the
Genetics of Alcoholism (COGA).
Date: April 29, 2019.
Time: 8:30 a.m. to 5:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, Main
Conference Hall, 6700A Rockledge Drive,
Bethesda, MD 20817.
Contact Person: Beata Buzas, Ph.D.,
Scientific Review Officer, National Institute
on Alcohol Abuse and Alcoholism, National
Institutes of Health, 6700B Rockledge Drive,
Room 2116, Bethesda, MD 20852, 301–443–
0800, bbuzas@mail.nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.271, Alcohol Research
Career Development Awards for Scientists
and Clinicians; 93.272, Alcohol National
Research Service Awards for Research
Training; 93.273, Alcohol Research Programs;
93.891, Alcohol Research Center Grants;
93.701, ARRA Related Biomedical Research
and Research Support Awards, National
Institutes of Health, HHS)
Dated: March 11, 2019.
Melanie J. Pantoja,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2019–04852 Filed 3–14–19; 8:45 am]
BILLING CODE 4140–01–P
VerDate Sep<11>2014
16:53 Mar 14, 2019
Jkt 247001
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended, notice is hereby given of the
following meetings.
The meetings will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended. The grant applications and
the discussions could disclose
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning
individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
Name of Committee: Center for Scientific
Review Special Emphasis Panel; Member
Conflict: Autism and Other
Neurodevelopmental Disorders.
Date: March 26, 2019.
Time: 10:00 a.m. to 2:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892
(Virtual Meeting).
Contact Person: Samuel C. Edwards, Ph.D.,
Chief, BDCN IRG, Center for Scientific
Review, National Institutes of Health, 6701
Rockledge Drive, Room 5210, MSC 7846,
Bethesda, MD 20892, (301) 435–1246,
edwardss@csr.nih.gov.
This notice is being published less than 15
days prior to the meeting due to the timing
limitations imposed by the review and
funding cycle.
Name of Committee: Center for Scientific
Review Special Emphasis Panel; Toxicology
and Digestive, Kidney and Urological
Systems AREA Review.
Date: April 3, 2019.
Time: 2:00 p.m. to 4:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892
(Telephone Conference Call).
Contact Person: Ganesan Ramesh, Ph.D.,
Center for Scientific Review, National
Institutes of Health, 6701 Rockledge Drive,
Room 2182 MSC 7818, Bethesda, MD 20892,
301–827–5467, ganesan.ramesh@nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.306, Comparative Medicine;
93.333, Clinical Research, 93.306, 93.333,
93.337, 93.393–93.396, 93.837–93.844,
93.846–93.878, 93.892, 93.893, National
Institutes of Health, HHS)
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Dated: March 12, 2019.
Sylvia L. Neal,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2019–04850 Filed 3–14–19; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
The National Institutes of Health
‘‘Methods and Measurement in Sexual
& Gender Minority Health Research:
Identifying Research Opportunities’’
ACTION:
Request for comments.
Sexual and gender minority
(SGM) is an umbrella phrase that
encompasses lesbian, gay, bisexual, and
transgender populations as well as those
whose sexual orientation, gender
identity and expressions, or
reproductive development varies from
traditional, societal, cultural, or
physiological norms. This includes
Disorders or Differences in Sex
Development (DSD), sometimes known
as intersex.
The Sexual & Gender Minority
Research Office (SGMRO) at the
National Institutes of Health (NIH) has
developed the document ‘‘Methods and
Measurement in Sexual & Gender
Minority Health Research: Identifying
Research Opportunities’’ pertaining
specifically and exclusively to methods
and measurement research in SGM
health research. Experts in the field
identified research opportunities related
to methods and measurement in SGM
health research during a workshop held
in the Spring of 2018. The document
reflects the content of the discussion
among participants at the Methods and
Measurement in SGM Health Research
Workshop and does not represent an
official position of NIH or any other
government agency. We would like to
obtain comment on the specifics of this
document to consider for the purposes
of informing and enhancing its content.
DATES: To ensure consideration of your
comments, responses must be received
by April 15, 2019.
ADDRESSES: Responses to this notice
must be submitted electronically by
email to sgmhealthresearch@od.nih.gov.
Please use the subject ‘‘Comments:
Measurement.’’
SUMMARY:
Dr.
Karen Parker, Division of Program
Coordination, Planning, and Strategic
Initiatives, Office of the Director, NIH,
Building 1, Room 257, 1 Center Drive,
FOR FURTHER INFORMATION CONTACT:
E:\FR\FM\15MRN1.SGM
15MRN1
Agencies
[Federal Register Volume 84, Number 51 (Friday, March 15, 2019)]
[Notices]
[Pages 9537-9538]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-04856]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Proposed Collection; 60-Day Comment Request; Center for Cancer
Training (CCT) Application Form for Electronic Individual Development
Plan (eIDP) (National Cancer Institute)
AGENCY: National Institutes of Health, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: In compliance with the requirement of the Paperwork Reduction
Act of 1995 to provide opportunity for public comment on proposed data
collection projects, the National Institutes of Health, National Cancer
Institute (NCI) will publish periodic summaries of propose projects to
be submitted to the Office of Management and Budget (OMB) for review
and approval.
DATES: Comments regarding this information collection are best assured
of having their full effect if received within 60 days of the date of
this publication.
FOR FURTHER INFORMATION CONTACT: To obtain a copy of the data
collection plans and instruments, submit comments in writing, or
request more information on the proposed project, contact: Erika
Ginsburg, Scientific Program Analyst, Center for Cancer Training,
National Cancer Institute, 9609 Medical Center Drive, Room 2W-106,
Bethesda, Maryland, 20892 or call non-toll-free number (240) 276-5627
or Email your request, including your address to:
ginsbure@mail.nih.gov. Formal requests for additional plans and
instruments must be requested in writing.
SUPPLEMENTARY INFORMATION: Section 3506(c)(2)(A) of the Paperwork
Reduction Act of 1995 requires: Written comments and/or suggestions
from the public and affected agencies are invited to address one or
more of the following points: (1) Whether the proposed collection of
information is necessary for the proper performance of the function of
the agency, including whether the information will have practical
utility; (2) The accuracy of the agency's estimate of the burden of the
proposed collection of information, including the validity of the
methodology and assumptions used; (3) Ways to enhance the quality,
utility, and clarity of the information to be collected; and (4) Ways
to minimizes the burden of the collection of information on those who
are to respond, including the use of appropriate automated, electronic,
mechanical, or other technological collection techniques or other forms
of information technology.
Proposed Collection Title: Center for Cancer Training (CCT)
Application Form for electronic Individual Development Plan (eIDP),
0925-XXXX, Exp., Date XX/XXXX, NEW, National Cancer Institute (NCI),
National Institutes of Health (NIH).
Need and Use of Information Collection: This information collection
request is to approve the electronic Individual Development Plan (eIDP)
for three years. The National Cancer Institute's (NCI) Center for
Cancer Training (CCT) supports NCI's goal of training cancer
researchers with various educational levels (postbaccalaureate,
graduate students, postdoctoral fellows) and for varying periods of
time (3 months to 5 years). The eIDP is an online, detailed
questionnaire focused on responses to career and professional goals and
expectations while the trainee works at the NCI. The eIDP ensures the
NCI trainees are receiving proper career and professional guidance,
making appropriate progress, and determining activities to achieve
their goals. The eIDP is also used to track trainees' career and
professional goals and to ensure trainees receive the tools needed to
achieve those goals. It is expected the trainees will complete the eIDP
annually and that the eIDP process could be improved by their
responses. The effectiveness of training could also be enhanced by the
reports received by the trainees completing the eIDP. Individual
Development Plans have been collected by paper and pencil from trainees
since 2001. With the implementation of the electronic system, a pilot
of the eIDP was approved by OMB (#0925-0046) and implemented in
December 2018. The pilot improved the clarity of the instructions for
the eIDP system, and incorporated feedback from the trainees to improve
the overall trainee IDP experience, which advances the effectiveness of
training.
OMB approval is requested for 3 years. There are no costs to
respondents other than their time. The total estimated annualized
burden are 1,209 hours.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average time
Type of respondents Number of responses per per response Total annual
respondents respondent (in hours) burden hours
----------------------------------------------------------------------------------------------------------------
Individuals--Trainees........................... 1,000 1 1 1,000
Individuals--Alumni............................. 500 1 5/60 42
Individuals--Feedback........................... 500 1 20/60 167
---------------------------------------------------------------
Total....................................... 1,000 1,000 .............. 1,209
----------------------------------------------------------------------------------------------------------------
[[Page 9538]]
Patricia M. Busche,
Project Clearance Liaison, National Cancer Institute, National
Institutes of Health.
[FR Doc. 2019-04856 Filed 3-14-19; 8:45 am]
BILLING CODE 4140-01-P