Delegation Log In Clinical Trials

Jul 17, 2015 · Delegation of Authority Log. Purpose: To record all study staff members’ significant study-related duties. Audience/User: Principal investigators (PIs), study coordinators, other site staff, clinical monitor. Details: This log should provide a comprehensive list of study staff members and the duties that have been delegated to them by the PI.

Site Signature and Delegation of Responsibilities Log . ... clinical trials”. ... • If satellite sites are involved in the trial, each site should maintain their own delegation log to ensure timely and accurate completion with a copy maintained at the main site.

Delegation of Authority Log lists all of the study staff, including the Investigators and Clinical Research Coordinators (CRCs), and other designated site personnel who are delegated significant trial-related duties from the PI. The DOA Log must be completed for all therapeutic and non-therapeutic clinical trials (i.e., Investigator-Initiated,

Oct 24, 2014 · There is a lot of discussion on message boards and even more discussion within the clinical research industry surrounding Delegation of Authority logs. The first item I would like to discuss is the purpose of the delegation of authority log.

During their recent webinar on best practices for maintaining ethical and compliant delegation of authority (DOA) at research institutions, presenters Wendy Tate and Mariette Marsh discussed methods and tools to adequately navigate oversight of research operations in an increasingly complex clinical trial landscape.The two presenters received many attendee questions regarding the completion ...

As monitors, we come across this question from time to time…Is a Delegation log required? The principal investigator is ultimately responsible for the conduct of the study, but it is common for the PI to delegate certain study-related tasks to other members of the research team (co …

FDA’S 2014 Clinical Investigator Training Course . Cynthia F. Kleppinger, M.D. Investigator Responsibilities – Regulation and Clinical Trials

the Site Signature and Delegation of Responsibilities Log and number pages accordingly (3a,3b,etc). » If satellite sites are involved in the study please discuss with your Sponsor how best to

Search All Clinical Research Use this field to search all clinical research documents. ... Documenting Delegation of Authority outline the process for documenting delegation of authority for DF/HCC clinical trials. ... DF/HCC Policy Training and Signature Record Log DF/HCC Key: Delegation of Tasks for Clinical Research List

Site Signature Log - Delegation of Authority Log ( MS Excel, 47K or screen-readable PDF, 294K) A record of all study personnel and their specific responsibilities, signatures, and dates of involvement during the conduct of a clinical research study.