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Centralized Reporting Portal Technical Requirement Suggestions

A single, central reporting portal for all reporting would help achieve the goals of the DATA Act. A central portal should provide the following functions: 1) One Portal a. The goal is to have one place for recipients to report on research expenditures. b. All the agencies conform from the beginning. i. If exceptions are granted, it should be clearly documented who has been granted an exception and, the length of time ...more »

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DATA Act Implementation: Four Guiding Principles

Enactment of the Digital Accountability and Transparency Act in May, 2014 provides many opportunities for the Office of Management and Budget and the Department of Treasury to improve the public transparency of Federal spending while simultaneously reducing the overall reporting burden on both Principal Investigators and institutional Research Administrators. However, there are also many implementation scenarios that ...more »

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Allow 120 Days for ALL Fnl Rprt’g (Fncl & Prgr) for ALL agencies

Change UG to Allow 120 Days for all Final Reporting (Financial and Programmatic) for all agencies Currently the Uniform Guidance (UG) requires that all financial & programmatic reports are submitted to the sponsor within 90 days after end date. Several agencies, through coordination with the FDP (Federal Demonstration Partnership) and COGR, are adjusting their deadlines to 120 days after end-date. These agencies, most ...more »

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48 votes
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Effort Reporting

Effort Reporting should be incorporated into the progress reports. some sponsors want person months and descriptions of person(s) tasks.

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Conflict of Interest

Right now the federal conflict of interest statements are due at the application and then reconfirmed upon award. Since most grants aren't funded, it would save hours of time to not have this due until the Just in time documents.

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PubMed

The requirement to list PubMed Central ID #s is a HUGE time and effort burden for research administrators. That is the #1 requirement I would change. There must be other ways to track compliance with the Public Access Policy.

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RPPR Burden

For each person paid from the grant who worked >160 hours (1 person month) during the grant year, there must be a Commons ID (including the completion of Personal Profile Information). There also needs to be information about the total number of hours each person worked on the grant during grant year so that person months can be calculated. This information is required for undergraduate who may be paid hourly as student ...more »

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True single audit

1. Achieve a true single audit. IHEs are still subject to multiple audits of their individual programs and compliance processes, despite the Single Audit Act of 1984, OMB Circular A-133 and 2CFR-200 Uniform Guidance which mandate single audits for non-federal entities that receive federal funding. The University is subject to a major compliance audit, desk audits and program audits each year.

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True single audit

1. Achieve a true single audit. IHEs are still subject to multiple audits of their individual programs and compliance processes, despite the Single Audit Act of 1984, OMB Circular A-133 and 2CFR-200 Uniform Guidance which mandate single audits for non-federal entities that receive federal funding. The University is subject to a major compliance audit, desk audits and program audits each year.

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IRB and IACUC Review

2. Eliminate Two Layer IRB and IACUC Review of Human and Vertebrate Animal Research - Institutions receiving federal funds for research with human subjects or vertebrate animals are required to maintain a Federal-wide Assurance (FWA) or Animal Welfare Assurance (AWA) with the DHHS Office of Human Research Protections (OHRP) or Office of Laboratory Animal Welfare (OLAW), respectively. Institutions thereby accept the responsibility ...more »

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Harmonize Training

Harmonize Requirements and Standardized Collection of Non-Financial Training Prior to Issuance of an Award - Non-Financial Investigator training requirements (e.g. Financial Conflict of Interest, Responsible Conduct of Research, Research with Human Subjects), are convoluted because acceptable subject matter and timelines for completion vary by agency. Non-financial training requirements should be harmonized to reduce ...more »

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