Author: Jessica

Individual Participant Data (IPD) Sharing Statement

The International Committee of Medical Journal Editors (ICMJE) requires that an IDP Sharing Statement be include in the ClinicalTrials.gov registration. Download the Guidance for Completing the IPD Sharing Statement on ClinicalTrials.Gov (PDF).

Joint Research Office for Contracts Metrics

This graph encompasses only new Industry Clinical Trial Agreements. This graph incorporates data from all contracts processed by JROC related to industry clinical trials (e.g. Clinical Trial Agreements, Confidentiality Agreements, Amendments, Service Agreements related to a Clinical Trial, etc.). Awaiting Intake represents the average time JROC is awaiting documentation needed to begin negotiations. With Department […]

RMS PD/PT In-Person Training Opportunities

The current schedule of all RMS in-person training and drop-in sessions can be found in the RMS section of the Research Education Calendar. RMS 101: Budget and Routing Prerequisites Completion of applicable training in Learn@Work (see RMS Training in Learn@Work above) RMS 101 Worksheet RMS 102: Advanced Submissions and Proposal Tracking Prerequisites Attendance of RMS 101 […]

Running Note

Investigators and coordinators have found a running note to be an effective way to document interactions with participants. This document should be an ongoing record that is signed and dated as each entry is made. Items noted on this type of document are phone call conversations, items to watch for during the next study visit, […]