Sexual Harassment

Sexual harassment, including sexual violence, is a form of sex discrimination and is prohibited under Title IX. Unwelcome sexual advances, requests for sexual favors, and other verbal, and nonverbal or physical conduct of a sexual nature constitute sexual harassment when this conduct is so severe, persistent or pervasive that it affects an individual’s employment, unreasonably interferes with an individual’s work or educational performance, or creates an intimidating or hostile work or educational environment. All sexual harassment concerns are handled by the Title IX office.

According to Texas A&M System Regulation 08.01.01 and Texas State Law, all employees (except for confidential employees) who experience, observe, or become aware of alleged discrimination, harassment, or related retaliation must promptly report the incident(s) to the Designated Official at Tarleton State University. Information on mandatory reporting can be found here.

Reporting can be done through contacting the Title IX/Civil Rights office, by filing a civil rights complaint, or submitting a report to TAMUS through EthicsPoint. See something, say something!

Federal Sponsor Policies

National Science Foundation

NSF Requirements & Policies
Off-Campus
Travel and Conference Grants
Subawardees

When Tarleton State University is a subawardee or non-lead institution under an NSF award: Notifications of Type 1 and Type 2 Harassment Decisions will be made directly to NSF by the appointed AOR of Tarleton, per current NSF guidance.  However, the University may also communicate with the prime awardee as necessary or appropriate under the circumstances.

Executed subaward agreements, where TSU is the Prime Awardee: The subawardee must notify NSF of any PI or co-PI violations of Type 1 and Type 2 Harassment Decisions per 83 FR 47940, which states “If a coPI is affiliated with a subawardee organization, the AOR of the subawardee must provide the requisite information directly to NSF“. The subawardee of the institution is not required to report to Tarleton State University as the prime awardee unless deemed appropriate by the subawardee institution.

Language to be included in NSF Subawards: The PI and any co-PI(s) identified on an NSF award are in a position of trust. These individuals must comport themselves in a responsible and accountable manner during the award period of performance, whether at the awardee institution, on-line, or at locales such as field sites, facilities, or conferences/workshop.  For all co-PIs of subawards, the Authorized Organizational Representative of the subawardee must provide the requisite information directly to NSF on co-PIs’ violations of awardee policies, codes of conduct, statutes, regulations or executive orders related to sexual harassment, other forms of harassment or sexual assault consistent with NSF requirements in 83 FR 47940.

Reporting

DHHS: NIH

DHHS/NIH Requirements & Policies
Reporting

Institutional Reporting

NIH recipient institutions are required to notify NIH when individuals identified as PD/PI or other Senior/Key personnel in an NIH notice of award are removed from their position or are otherwise disciplined by the recipient institution due to concerns about harassment, bullying, retaliation or hostile working conditions. (NOT-OD-22-129)

Are you an institutional official who needs to report that an individual identified as PD/PI or other Senior/Key personnel has been removed from their position or otherwise disciplined due to concerns about harassment, bullying, retaliation or hostile working conditions? Learn how to report the action and what happens when you do. Note, the procedures below are effective July 9, 2022. See NOT-OD-20-124

Standard Procedure

flow chart process described on page
  1. Authorized Organization Official of recipient institution notifies NIH within 30 days of disciplinary action being taken. Notifications must include, at a minimum:
    • The name of the Authorized Organization Representative submitting the notification
    • The name of the individual of concern
    • A description of the concerns
    • The action(s) taken
    • Any anticipated impact on the NIH-funded award(s).
  2. NIH’s Office of Extramural Research (OER) assesses the report, checking for whether:
    1. Staff are key personnel on an NIH-funded grant. If NIH-funded grants are involved whether the person of concern is involved in and should be removed from peer review service

    Notification is done via this web form: Notify NIH
  3. OER may reach out to the institution to better understand
    1. If an institutional investigation commenced; if there was a finding
    2. The impact, if any, on NIH research
    3. If any identified risks to research staff and/or students have been mitigated
    4. Actions taken and safeguards that have been put in place
    5. Other factors and actions relevant to the allegation
  4. Appropriate actions are taken to ensure NIH-funded research is occurring in a safe environment. These actions may include, but are not limited to:
    1. Coordinating with funding NIH Institute on necessary grants management actions, which may include requesting the recipient institution identify a replacement principal investigator on the award
    2. Holding pending awards associated with the PI of concern while compliance issues are resolved
    3. Declining to approve requests to transfer grants involving the PI to another institution
    4. Requiring special reporting requirements from the institution
    5. Requiring follow-ups with institutions to ensure issues have been fully addressed

Responsible Conduct of Research Training

Tarleton State University requires all faculty, staff and students eligible to conduct research be trained in Responsible Conduct of Research (RCR). All research eligible individuals must take the Collaborative Institutional Training Institute “CITI” RCR course. This requirement is in addition to any other RCR training. Research eligible individuals who have taken the CITI RCR course within the last five years at a previous institution do not need to retake the course. 

Access to certain university processes related to research for all faculty, staff and students who have not yet completed RCR training, will be suspended until the RCR training is completed. This includes, but not limited to, submission of IBC, IRB, and IACUC protocols and amendments.

CITI RCR Course

There are several discipline-specific courses that consist of an introduction, basic foundation text, embedded case studies, and quiz questions.

  • Biomedical Research
  • Social and Behavioral Research
  • Biosafety
  • Animal-specific courses
  • IACUC Requirements

CITI allows users to select more than one discipline-specific course when you first log in and register to take the RCR course. CITI automatically combines the unique modules for the disciplines selected when generating the modules for users training.

Review of the required materials and completion of the quizzes will take about 30-35 minutes per topic. Courses do not have to be completed in one session. A minimum, aggregate score of 80% is required to pass the RCR course. CITI allows users to retake the quizzes if the minimum score was not obtained to pass the course.

Upon course completion, a copy of the completion certificate will be available to print and retain for your records. The CITI system keeps track of all completion data, and Tarleton State accesses completion data directly from CITI.

Federal Sponsor Requirements

NSF

NSF requires universities to certify that it has a plan to provide appropriate training and oversight in the responsible and ethical conduct of research to undergraduates, graduate students, and postdoctoral researchers who receive NSF support to conduct research. Certification of University compliance is done by an authorized Tarleton State representative as part of the institutional proposal approval process (e.g., when a sponsored program officer submits the proposal in FastLane). Specific instructions are found in Chapter IV.B Responsible Conduct of Research (RCR) of the NSF Proposal and Award Policies and Procedures Guide.

All students and postdoctoral researchers supported by NSF sponsored projects must complete the CITI online course in the Responsible Conduct of Research within 60 days of appointment.  The PI is responsible for ensuring that all students and postdocs complete the CITI RCR course and begin a dialogue on the responsible conduct of research. The PI is also required to complete the CITI RCR training.  PI’s should not include any specific information on RCR training within proposals. NSF does not want program details – only the institution’s certification that there is a program in place.

Training records are subject to monitoring by NSF auditors.

NIH
NIFA

Clinical Trials

Effective January 1, 2017 – NOT-OD-16-148 states the NIH expects all NIH-funded clinical investigators and clinical trial staff who are involved in the design, conduct, oversight, or management of clinical trials to be trained in Good Clinical Practice (GCP). Recipients of GCP training are expected to retain documentation of their training. GCP training should be refreshed at least every three years in order to stay up to date with regulations, standards, and guidelines.

NOT-OD-16-148​: Policy on Good Clinical Practice Training for NIH Awardees Involved in NIH-funded Clinical Trials

The principles of Good Clinical Practice (GCP) help assure the safety, integrity, and quality of clinical trials by addressing elements related to the design, conduct, and reporting of clinical trials. GCP training describes the responsibilities of investigators, sponsors, monitors, and IRBs in the conduct of clinical trials. 

GCP training aims to ensure that:

  • the rights, safety, and well-being of human subjects are protected
  • clinical trials are conducted in accordance with approved plans with rigor and integrity
  • data derived from clinical trials are reliable

The policy does not require a particular GCP course or program. Training in GCP may be achieved through a class or course, academic training program, or certification from a recognized clinical research professional organization. Tarleton strongly suggests taking the NIH training that is free of charge when applying for federal funding for clinical trials, including:

All clinical trials must undergo an IRB review and comply with university, system, local, state, and federal human subject research policies.