Author: Corinne Rogers
Date: 06-22-10 18:55
DEPARTMENT: Institutional Review Board
DUTIES: The individual will be responsible for a range of activities within the Office of Human Subjects Research and the Institutional Review Board. These include research compliance monitoring, consent observation, protocol observation, chart reviews, adverse event tracking and reviews, consultation with investigators and related data entry, analysis and reports. The individual will also assist in the writing of IRB website content, content and guidance for IRB online applications, and in researching and developing regulatory policies and procedures.
EDUCATION: A Master’s degree is preferred.
TRAINING and Experience: The individual must be familiar with human subjects protection and Institutional Review Board functions, have outstanding writing skills, and have relevant experience in clinical research coordination, audit or oversight.
For full Consideration, apply online at http://rfmh.iapplicants.com/ViewJob-87801.html .
|
|
