Clinical Trials Resource Center

Conducting Clinical 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?

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?

Safety Reporting - What should be reported? To whom? How quickly?

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.