Conducting Trials

Get started here finding helpful forms and guidelines for all your research needs.

Protocol Development -  What should be in your protocol? Go here to find templates, outlines and guidelines.

Consent Development - What elements have to be covered? What is the latest required UT-IRB language?

Budgeting & Billing - For what expenses should you plan? What will be required from the Office of Sponsored Projects?

Research Participant Payment (1099) Guidelines - When should you collect W-9 information from participants who are being paid for participation in research? 

Recruitment Strategies - Now that you've developed your protocol and consent, how do you plan to get subjects?

Data and Safety Monitoring -When do you need a Data Safety Monitoring Plan? A Data Safety Monitoring Board?  Who forms the board?

Quality Management - What are GCP Guidelines for conducting a quality clinical trial?

Study Management - The day-to-day study coordinator experience from pre-study initiation to subject management and drug accountability -get your tips and template forms here.

Lab Certificates - If you will be working with a local lab during the course of clinical trial, then you may need to keep current CAP and CLIA certificates in your regulatory binder. If you need a copy of MHH lab certificates,  please, contact the MHH CIRI Research Specialist that is assigned to your trial.  

ADDITIONAL RESOURCES

COMMITTEE FOR THE PROTECTION OF HUMAN SUBJECTS | ANIMAL RESEARCH | ENVIRONMENTAL HEALTH & SAFETY | CLINICAL RESEARC UNIT | CENTER FOR CLINICAL AND TRANSLATIONAL SCIENCE | BIOSTATISTICS, EPIDEMIOLOGY AND RESEARCH DESIGN | CORE LABORATORIES | SPONSORED PROJECTS | TECHNOLOGY MANAGEMENT
OFFICE OF RESEARCH 

Clinical Trials Resource Center (CTRC)
7000 Fannin Street, Suite 795
Houston, Texas 77030
phone 713-500-3622
fax 713-500-0334
[email protected]