Clinical Research Education Course - Basic
This educational program is designed and conducted by experienced clinical trial research professionals from within UT Health. The program examines the entire clinical trial process, from planning to trial close-out activities, and provides practical recommendations for increasing the efficiency of clinical trial conduct at investigative sites. This program combines didactic presentations and interactive group sessions.
Day 1 focuses on financial management and includes presentations on basic financial principles, research contracting, budget development and billing process.
**Day 2 includes discussion about human subject protections, GCP principles, institutional compliance and consent process.
**Day 3 includes presentations on study initiation, study conduct, documentation, investigational devices and drugs and reporting requirements.
**To get the most from this course, please be sure you have completed your CITI Protection of Human Subjects Training.
Objective: To provide a model of practice in conducting clinical research based on the principles of Good Clinical Practice, thereby focusing on research compliance, protecting the safety and well-being of the research subject and ensuring integrity of the research
Audience: Investigators, research nurses, research coordinators.
*****REGISTRATION NOT OPEN*****
Dates : October 2013
Location: Cooley University Life Center, 7440 Cambridge St, Houston 77054
COURSE FEES
Please note course fees for UT Health and MHH participants:
Day 1 - $50
Day 2, 3 - $100
Day 1, 2, 3 - $150
Course fees for non-UT Health/MHH participants:
Day 1 is not open to outside participants.
Day 2 + 3 - $600
Questions?
OFFICE OF RESEARCH | CLINICAL TRIALS RESOURCE CENTER |
COMMITTEE FOR THE PROTECTION OF HUMAN SUBJECTS |ANIMAL RESEARCH | ENVIRONMENTAL HEALTH & SAFETY | CORE LABORATORIES | SPONSORED PROJECTS | TECHNOLOGY MANAGEMENT
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Clinical Trials Resource Center (CTRC) last modified March 21, 2013 |
