Participating in Clinical Trials

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Home > Professional Education > Women's Leadership Initiative > Business of EP > Participating in Clinical Trials

Participating in Clinical Trials

These presentations outline the process for identifying and becoming involved in multi-institution clinical trials, including sources of grants and tips for obtaining NIH grants. The process of using clinical trial data for sub-study analysis and hypothesis-generating for future prospective trials is also covered.

Participating in Multi-Center Clinical Trials

This session was presented at the Heart Rhythm 2008 Annual Scientific Sessions.
May 13-16, 2008
San Francisco, CA

Chair

Jeanne Poole, MD

Presentations and Faculty

The Language of the NIH: Types of Studies, NIH Funding and the NIH Process
Anne Mascette, MD

The Devil is in the Details: The IRB and Other Site Study Issues
Karen Friday, MD

Breaking into Clinical Trial Participation: Substudies, Committees and Becoming a Site Investigator
Marye Gleva, MD

Tools of the Trade: Statistical Realities
Christine Albert, MD

Wrap-Up
Jeanne Poole, MD

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Participating in Multi-Center Clinical Trials