Registration for the NCI Workshop on Rational Drug Discovery

Sub-Study NCI Rationale Drug Discovery Workshop.docx

Conference, Meeting, Workshop, and Poster Session Registration Generic Clearance (OD)

Registration for the NCI Workshop on Rational Drug Discovery

OMB: 0925-0740

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Request for Approval under the Generic Clearance for the “Conference, Meeting, Workshop, and Poster Session Registration Generic Clearance (OD)”(OMB#: 0925-0740, Expiration Date: 07/31/2022)


Shape1 TITLE OF INFORMATION COLLECTION: Registration for the NCI Workshop on Rational Drug Discovery


PURPOSE: In line with guidance from the National Cancer Advisory Board (NCAB) Ad Hoc subcommittee on Experimental Therapeutics to explore ‘Intelligent drug discovery based on biochemistry, structure, and mechanisms, including artificial intelligence-driven drug discovery’, the Developmental Therapeutics Program (DTP) at NCI is organizing a 2-day virtual meeting exploring these topics.  Our goals are to engage expert stakeholders to assess the state of the field and learn where ‘bottlenecks’ or ‘gaps’ exist that are preventing use/implementation of priority areas, and identify opportunities for NCI to apply support that will drive advances in these areas. Workshop will be conducted virtually on October 18-19 2021.


Session topics will include:

  • Structural Biology.   

  • Novel Therapeutic Modalities.   

  • Target Interrogation.  

  • Artificial Intelligence (AI) and Machine Learning (ML) in drug discovery 


DESCRIPTION OF RESPONDENTS: PIs/researchers, clinicians, and trainees (postdocs, fellows, and medical/graduate students) from government, academia, and industry


TYPE OF COLLECTION:


[ ] Abstract [ ] Application

[X] Registration Form [ ] Other: ______________________


CERTIFICATION:


I certify the following to be true:

  1. The collection is voluntary.

  2. The collection is low-burden for respondents and low-cost for the Federal Government.

  3. The collection is non-controversial and does not raise issues of concern to other federal agencies.



Name: Anju Singh





To assist review, please provide answers to the following question:


Personally Identifiable Information:

  1. Is personally identifiable information (PII) collected? [X] Yes [ ] No

  2. If Yes, is the information that will be collected included in records that are subject to the Privacy Act of 1974? [X] Yes [ ] No


Gifts or Payments:

Is an incentive (e.g., money or reimbursement of expenses, token of appreciation) provided to participants? [ ] Yes [X] No


Amount: N/A


Explanation for incentive: N/A


ESTIMATED BURDEN HOURS and COSTS


Category of Respondent

No. of Respondents

No. of Responses per Respondent

Time per Response

(in hours)

Total Burden

Hours

Individuals

500

1

5/60

42

Totals


500


42



Category of Respondent

Total Burden

Hours

Hourly Wage Rate*

Total Burden Cost

Individuals

42

$48.45

$2,034.90

Total



$2,034.90

*Source of the mean Hourly Wage Rate is provided by the Bureau of Labor Statistics, Occupation title “Medical Scientists” 19-1040, https://www.bls.gov/oes/2020/May/oes_nat.htm#00-0000.



FEDERAL COST: The estimated annual cost to the Federal government is $1,348.


Staff

Grade/Step

Salary**

% of Effort

Fringe

(if applicable)

Total Cost to Gov’t

Federal Oversight






Program Director

14/4

$134,782

1%


$1,348

Contractor Cost





$0

Travel





$0

Other Cost





$0

Total





$1,348

**The salary in the table above is cited from https://www.opm.gov/policy-data-oversight/pay-leave/salaries-wages/salary-tables/21Tables/html/DCB.aspx




The selection of your targeted respondents


  1. Do you have a customer list or something similar that defines the universe of potential espondents and do you have a sampling plan for selecting from this universe? [ X ] Yes [ ] No


If the answer is yes, please provide a description of both below (or attach the sampling plan)? If the answer is no, please provide a description of how you plan to identify your potential group of respondents and how you will select them?


Respondents will be register from targeted lists of PIs/researchers, clinicians, and trainees (postdocs, fellows, and medical/graduate students) from government, academia, and industry and advertisements using various social media platforms like Linkedln, NCI Twitter, news letters, etc.






Administration of the Instrument


How will you collect the information? (Check all that apply)

[X] Web-based or other forms of Social Media

[ ] Telephone

[ ] In-person

[ ] Mail

[ ] Survey Form

[ ] Chart Abstraction

[ ] Other, Explain


Will interviewers, facilitators, or research coordinators be used? [ ] Yes [X] No


Please make sure that all instruments, instructions, and scripts are submitted with the request.


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File Typeapplication/vnd.openxmlformats-officedocument.wordprocessingml.document
File TitleGeneric Clearance Submission Template
SubjectGeneric Clearance Submission Template
AuthorOD/USER
File Modified0000-00-00
File Created2022-02-14

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