Appendix: Considerations for Faculty and Principal Investigators

Three different hats hanging side by side on separate wooden hooks in a dim hallway

Three hats on three hooks in one hallway: a faculty researcher is an author, an instructor, and a supervisor, and each role carries its own AI-use obligations.

The five days of this workshop are written from the standpoint of a researcher acting as an author: writing, coding, reviewing literature, and publishing. A faculty member holds three further roles that the daily curriculum does not address directly, each of which carries its own AI-use considerations: writing grant proposals under a funder’s specific rules, setting AI policy for the students and trainees they teach, and supervising the research (and resolving the authorship questions) of graduate students and postdocs who are themselves using AI tools. This appendix extends the workshop’s verify-and-disclose discipline into those three roles.

Grant writing and funder-specific AI policy

Day 5’s ethics section covers the reviewer side of grant funding: NIH’s outright prohibition on generative AI in its peer-review process, adopted to protect the confidentiality of applicants’ unpublished ideas (National Institutes of Health, Office of Extramural Research, 2023). The applicant side of the same funding relationship carries a separate and, as of this writing, still-evolving set of rules that a faculty PI needs to track independently, because it governs the proposal they are drafting, not the proposal they are reviewing.

The National Science Foundation requires, as of PAPPG 24-1 (effective for proposals due on or after May 20, 2024), that a proposer disclose the extent and manner of any generative AI use in preparing the proposal (National Science Foundation, 2024). A later supplement, effective December 8, 2025, sharpened the stakes considerably: NSF’s research-misconduct definition was amended to explicitly cover fabrication, falsification, or plagiarism committed through the use or assistance of AI-based tools (National Science Foundation, 2025). That amendment matters because it removes any ambiguity about whether AI-assisted misconduct is treated differently from misconduct committed unaided; it is not. A proposer who submits AI-fabricated preliminary data or an AI-fabricated citation is exposed to the same research-misconduct process as a proposer who fabricated it by hand.

NIH’s applicant-side policy, issued July 17, 2025 as NOT-OD-25-132 (“Supporting Fairness and Originality in NIH Research Applications”), takes a stricter substantive line than NSF’s disclosure-based approach: NIH states it will not consider an application, or a section of one, that is “substantially developed by AI” to be the applicant’s original idea, requires disclosure of AI-generated content, and backs the policy with AI-detection technology on submitted applications (National Institutes of Health, Office of Extramural Research, 2025). The same notice introduced an unrelated but simultaneously effective cap of six new, renewal, resubmission, or revision applications per principal investigator per calendar year, a reminder that funder policy in this area is moving quickly enough that a policy read a year ago may already be superseded.

The practical implication for a faculty PI is that “I disclosed my AI use” is not a uniform, portable compliance step across funders the way it functions across journals under ICMJE and COPE (Day 5). NSF’s rule is a disclosure requirement layered onto an unusually explicit misconduct exposure; NIH’s rule is closer to a substantive cap on how much of the intellectual content can be AI-produced at all, regardless of disclosure. A PI who applies to both agencies in the same year needs to check each notice directly, at proposal-drafting time, rather than assuming a disclosure practice adequate for one funder satisfies the other.

Where the efficiency actually is: boilerplate, not aims

A document tray holding a thick stack of papers in shadow, with one single sheet in front of it lit by a narrow warm spotlight

A thick stack in shadow beside one sheet under a spotlight: a proposal’s small core of original argument, surrounded by the required material no reviewer scores for creativity.

NIH’s “substantially developed by AI” standard is often read as a reason to avoid AI tools in proposal preparation altogether. That reading gives up a real and entirely compliant efficiency gain, because a competitive proposal is not a uniform document. It contains a small core of genuinely original intellectual content and a substantial surrounding mass of required, low-originality, high-volume material that every application needs and no reviewer scores for creativity.

The originality-bearing sections are the ones NIH’s policy is about: Specific Aims, Significance, Innovation, and the research strategy that makes the scientific case. These are the sections where an application is judged as the applicant’s own idea, and they are the ones to draft unaided. The surrounding material is different in kind: data-management and sharing plans, facilities and other resources, equipment descriptions, biosketch personal statements retargeted for each application, authentication of key resources, formatting and page-limit compliance checks. This material is required, repetitive, largely reused across applications, and carries no originality claim. Drafting it from prior applications and the specifics of the project at hand is exactly the kind of mechanical restructuring task that AI assistance handles well, in the same sense as the reviewer-response skeleton in Day 4.

Two cautions keep this on the right side of the line. First, disclosure obligations attach to the whole application, not only to the interesting parts: if the funder requires disclosure of the extent and manner of AI use, as NSF does (National Science Foundation, 2024), boilerplate assistance is part of what gets disclosed, and there is nothing costly about saying so. Second, “boilerplate” refers to the section’s function, and not to how carefully it must be read. A data-management plan is a commitment the institution will be held to, and an AI-drafted plan that misstates where data will be deposited, or how long it will be retained, creates a real compliance problem rather than merely an aesthetic one. Delegate the drafting; keep the review.

A useful practical test for whether a given proposal section is safe to delegate is the following. If a reviewer would score the section as evidence of the applicant’s scientific originality, it should be drafted unaided. If a reviewer would only check that the section is present, complete, and compliant, an AI assistant can draft it and the PI can verify it.

Teaching implications: setting AI policy for students

Every other section of this book treats the reader as an AI tool’s user. A faculty member is also, simultaneously, the person who decides what AI use is permitted in their own classroom, and who has to act when a student’s AI use crosses into academic dishonesty. That role reversal is not a minor variation on the material in Days 2 and 4; it is a distinct skill, because the faculty member is now applying the verification and disclosure judgment this book teaches to someone else’s work, under an institutional academic-integrity process rather than a personal writing or research discipline.

In my view, a syllabus AI policy is more useful to students, and more defensible in an integrity hearing, when it states affirmatively what is permitted rather than only what is forbidden, and when it varies by assignment rather than applying one blanket rule to an entire course. An instructor who permits AI-assisted brainstorming on a problem set but prohibits it on a proctored exam needs to say so on each assignment, and should not rely on a single course-wide sentence in the syllabus. The disclosure-norms discussion in Day 4 applies here in a mirrored form. Ambiguity in the instructor’s own policy produces exactly the same kind of undisclosed, contested AI use discussed in Day 4’s book-deal worked example, except that the faculty member is now the one who must adjudicate it rather than the one being accused.

When a suspected violation does arise, the same epistemic discipline this book has taught throughout applies directly. An AI-detection tool’s output is evidence, not proof: the same false-positive risk documented in Day 4’s discussion of the contested book-deal case applies to student writing, arguably with higher stakes, since a false accusation against a student can trigger a formal disciplinary process. A detector score warrants the treatment Day 2 recommends for an AI-produced citation: it is an unverified claim that must be corroborated (through a conversation with the student, a comparison against their earlier work, or independent evidence) before it is acted upon, and it is not a self-sufficient verdict.

IRB and human-subjects data in third-party AI tools

Day 5’s confidentiality discussion covers uploading an unpublished manuscript or proposal to a generative AI tool. A sharper version of the same risk arises when a faculty PI or a member of their research team pastes actual human-subjects data, such as raw interview transcripts, identifiable survey responses, or clinical notes, into a consumer AI tool to summarize, code, or analyze it. This is not merely a confidentiality courtesy, as the manuscript case is; for IRB-approved human-subjects research, it is a question of whether the data handling matches what was disclosed to, and approved by, the IRB in the first place.

University guidance on this point is now fairly consistent and worth taking at face value rather than assuming it does not apply to a “harmless” summarization task. The University of Chicago’s generative AI guidance prohibits using confidential data, explicitly including HIPAA-covered patient data, FERPA-covered student data, and not-yet-public research findings, with public generative AI tools absent a prior security and privacy review (University of Chicago, 2024). Yale’s guidance for health-sciences research is explicit that a vendor’s own marketing claim of “HIPAA-compliance” is not sufficient on its own; whether a given tool is actually approved for HIPAA-covered data is a determination made case-by-case by the relevant university and health-system committees, not by the tool’s own documentation (Yale University, 2024). The practical rule that follows from both is straightforward. A general-purpose AI tool should never be treated as authorized for identifiable human-subjects data unless the institution has specifically reviewed and approved that tool for that data, in writing, and regardless of what the tool’s own privacy page claims.

A locally run open-weight model, described in Day 1’s selection criteria, is worth considering here specifically. It keeps the data on hardware the institution already controls, which converts an approval question about a third-party vendor into an ordinary question about local computing practice (Ollama, 2026). It does not remove the IRB obligation described next, since the protocol still governs where data may be processed, but it removes the vendor from the problem entirely.

The IRB dimension adds a second, independent problem beyond confidentiality. An approved protocol specifies the data-handling and data-sharing plan a researcher committed to when the study was approved; uploading identifiable data to a third-party AI tool not named in that plan is a deviation from the approved protocol, reportable to the IRB in most institutions’ policies, independent of whether any actual harm resulted. A PI running a lab should treat this as a supervision responsibility, not only a personal one: a graduate student or research assistant who pastes interview transcripts into a consumer chatbot to speed up a coding pass may not realize they have created a protocol deviation, and the PI who set up the project’s data-handling practices is the person positioned to have prevented it, by stating explicitly, before the data is collected, which tools (if any) are approved for use on that specific dataset.

Authorship and credit disputes with trainees

Day 5’s authorship discussion, grounded in ICMJE and COPE, settles the question of whether an AI tool can be an author (it cannot) and states that human authors remain fully responsible for AI-assisted content (Committee on Publication Ethics, 2023; International Committee of Medical Journal Editors, 2025). It does not address a distinct and increasingly common friction point: a graduate student or postdoc used an AI tool substantially in drafting a paper, running an analysis, or synthesizing literature, and the question of how much credit that trainee should receive, or how the AI use should be represented in the author list and contribution statement, becomes a live disagreement between the trainee and their supervisor.

The Contributor Roles Taxonomy (CRediT), a community-owned taxonomy of fourteen specific contribution types now used by many journals including Elsevier’s, was built precisely to separate the question “what did each person actually do” from the question “who counts as an author,” on the premise that conflating the two is a recurring source of dispute (NISO (National Information Standards Organization), 2022). Applied to a trainee’s AI-assisted work, a CRediT-style breakdown can state plainly that a given trainee performed “formal analysis” and “writing – original draft” with the assistance of an AI tool for literature search and prose editing, without that assistance either inflating or erasing the trainee’s own claim to authorship credit. A recent analysis specifically proposes using CRediT to resolve authorship disputes at NIH-funded institutions, on the grounds that a contribution-based framework gives disputing parties (including a trainee and a supervisor who disagree about how much a given AI-assisted contribution counts) a shared vocabulary to reason from, rather than leaving the disagreement to compete unstructured intuitions about what “real” authorship requires (Partin & Hosseini, 2025).

The supervisory responsibility this creates is to set the expectation before the dispute arises, not after. A PI who tells a new graduate student, at the start of a project, which AI tools are acceptable for which tasks (matching this book’s own distinctions: editorial help is generally fine, substantive help needs disclosure and scrutiny, as developed in Day 4), and who states in advance how AI-assisted contributions will be represented in an eventual author-contribution statement, has converted a likely late-stage authorship argument into an early-stage, low-stakes policy conversation. Waiting until a manuscript is nearly finished to discover that a trainee used an AI tool far more heavily than the supervisor assumed is the predictable consequence of never having stated a policy in the first place.

Reconciling conflicting institutional policies

Four old measuring rulers of different materials laid side by side, their graduated scales visibly not aligning with one another

Four rulers side by side, their scales not aligning: a journal, a university, a funder, and an IRB measuring the same AI use by different standards.

Day 5’s homework (Problem 7) asks the reader to compare a single venue’s AI policy against the ICMJE and COPE baseline. A faculty PI running an externally funded human-subjects project is rarely governed by a single policy at all: a journal’s disclosure requirements, the university’s own AI-use policy, the funding agency’s proposal- and award-stage rules, and the IRB’s approved data-handling plan can all apply to the same piece of work simultaneously, and they do not always agree with each other on particulars such as where disclosure belongs, how much AI assistance is permissible, or which tools are approved for which data.

Unfortunately, there is no general legal or professional rule that resolves every such conflict automatically. From my perspective the workable default, consistent with the disclose-generously stance already argued for in Day 4, is to comply with whichever applicable policy is most restrictive on the specific point in question, and to disclose that this was done. If a university policy permits a category of AI use that an IRB-approved protocol’s data-handling plan does not name, the protocol governs for that project’s data, because it reflects a specific commitment made to research subjects and to the IRB rather than a general institutional default. If a funder’s disclosure requirement is more detailed than a journal’s, meeting the funder’s standard automatically satisfies the journal’s. The reverse is not guaranteed, so each policy warrants an explicit check rather than an assumption that a satisfied minimum transfers upward.

The audit habit from Day 5 extends naturally to this problem. For a multi-funder or multi-site project, a PI’s provenance log should record not only what the AI tools did and where, but also which policy governed which decision. Several bodies may later have a legitimate interest in that answer: a journal editor, a program officer, an IRB coordinator, or a university research-integrity office. A log of this kind lets the question be answered from the record rather than reconstructed under pressure. The discipline this workshop teaches for AI use itself turns out to generalize to the discipline of managing the AI policies that govern that use: write it down as it happens, and do not wait for a conflict to force the reconstruction.

In conclusion, three points are to be emphasized for the faculty reader. First, funder rules are not portable, and a disclosure practice adequate for one agency does not establish compliance with another. Second, the roles beyond authorship, namely instructor and supervisor, are best handled by stating a policy in advance rather than adjudicating one after a dispute or a protocol deviation has already occurred. Third, when several authorities govern the same work, the most restrictive policy on the point in question is the safe default, and the record of which policy governed which decision belongs in the provenance log alongside everything else.