Clinical Research: Why Get Involved and How to Do It Right by Gretchen Bowker
Sharing Lessons Learned in Building Research Capabilities at One Institution by Robert Plant
A Sponsor’s Perspective: What We Look for in a Good Clinical Trial Site by Kara Mezger
During this webinar, you’ll learn:
Multiple benefits of clinical research
Tactics and operational tips to help start or improve your research program
How to plan a practical approach to meet federal regulations as well as identifying characteristics that attract research sponsors to your practice or organization
The best practices of successful clinical research programs and review common pitfalls to avoid
This webinar will benefit CEOs, CNOs, physician practice management leaders, IRB administrators or board members, private practice site administrators, and research site personnel.
Registration Fee: $200 per site registration (includes one phone connection and one internet connection for unlimited participants in the same location)
Pearl IRB is an independent Institutional Review Board that provides comprehensive IRB services for sponsors, institutions, principal investigators, and CRO’s nationwide.We deliver quality and timely reviews that balance the interests of human subjects, sponsors, and institutions. Together, we will drive enhanced efficiency and value in clinical research.To learn more, please visit us atwww.pearlirb.com, call us at 317.278.4100, or emailinfo@pearlirb.com.
Featured Speakers Gretchen Bowker-the chief operating officer for Pearl IRB. She has over 25 years experience in the development of pharmaceuticals, biologics, and devices and is a recognized expert in regulatory issues, bioethics, and compliance. Gretchen has over 15 years experience at both Eli Lilly and Roche Diagnostics.
Kara Mezger – the associate director of clinical affairs at Zimmer and a seasoned device development leader. At Zimmer, Kara has led a team of clinical researchers that supports all clinical research activities and regulatory support documents for 510k class I-II and PMA devices.
Robert Plant – the director of the Parkview Hospital Research Center in Ft. Wayne. He serves Parkview Community Hospital, primary investigators, and sponsors by conducting high quality research programs. Robert has worked with large sponsors such as St. Jude Medical, Sanofi-Aventis, Merck, Genentech, Astra Zeneca, and Medtronic to deliver high quality clinical trials which have resulted in dozens of new innovations being launched into the marketplace.
Need assistance with an IRB review or clinical trials?
