Last Revised: June 11, 2024 OverviewContingent WorkersPre-Employment (Incoming Faculty/Researchers) ProcessPost-Employment (Departing Faculty/Researchers) ProcessFAQsContactsGuest ID Usage and Process Overview Contingent Workers is a broad category covering non-employees in Workday. Workday@WashU has established guidance and procedures on Contingent Workers for the University as a whole. This document is an expansion of that guidance specifically for research purposes. […]
Topic: Human Subjects Research
Guest WUSTL Key Guidance
In order for Non-WashU personnel to obtain the necessary training and security access, two options are available and primarily depends on the anticipated needs and role with WashU: Contingent Workers: Non-WashU person with direct involvement in WashU research, under an agreement to use WashU space/equipment for non-WashU purposes, or requiring WUSTL key access to a […]
Participate in Research Studies
Researchers often rely on volunteers to participate in their studies. The links below provide information on what it means to be a research study participant, and how to volunteer for a study at WashU. Participate in Clinical Trials at WashU COVID-19 Clinical Trails with the Division of Infectious Diseases Volunteer for Health is Washington University […]
OnCore Training
OnCore
OnCore Standard Operating Procedures
Monitoring Guidance and FAQs
See also: COVID-19 Monitoring Guidance Approved: June 24, 2020Administratively Revised: August 20, 2021 Purpose and Applicability Guidance Centralized Monitoring or Remote Monitoring On-Site Monitoring Monitoring of Multi-Centered PI-Initiated Trials Frequently Asked Questions (FAQs) Resources I. Purpose and Applicability Monitoring procedures have evolved in recent years due to advancements in technology. Washington University in St. Louis is […]
Self-Audit Toolkit
Internally monitoring and self-auditing human research studies is a valuable way for researchers to ensure that participants’ rights, safety and welfare are protected and that the research is conducted in accordance with the approved research plan and documented according to best practices. The Key Elements for Monitoring Adherence (PDF) guides researchers in a holistic review […]
FDA Audit Checklist
Download the FDA Audit Checklist: From Notification through Close-Out (DOC).
Protocol Templates for Clinical Trials (NIH Templates for both biomedical and behavioral & social sciences research involving human subjects)
See NIH protocol templates for both biomedical and behavioral & social sciences research involving human subjects.