June 9, 2011 – Integrating & Sustaining Clinical Research

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Indiana Hospital Association andPearl IRB invite you to a webinar:Integrating and Sustaining Clinical Research

June 9, 2011 from 3:00 – 4:30 P.M. EST.

Register Here

 

Featured Presentations

  • 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)

To learn more, click here.

 

About Pearl IRB

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.

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WEBINAR

 

Integrating and Sustaining Clinical Research

 

June 9, 2011

3:00- 4:30 P.M. EST

Register Now

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 Mezgerthe 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?

Contact Us 

Check out our Website and Blog atwww.pearlirb.com

 

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November 6, 2010 – Pearl IRB Speaking at the ACRP Excellence in Clinical Research Fall Symposium

Pearl IRB is speaking on a panel and exhibiting at the ACRP Excellence in Clinical Research Fall Symposium – REGISTER NOW!
Don’t miss the Circle City ACRP Event
held on November 6, 2010

Who should attend:

All personnel who are involved in or planning to be involved in clinical research. This conference is targeted for both new and experienced clinical research professionals including research nurses, clinical research coordinators, investigators, site managers, IRB members, and Pharmaceutical & Medical Device representatives.

What will be covered:

The pursuit of excellence in clinical research will be presented from the perspective of each of the major clinical research stakeholders. Click here for full agenda and brochure.

Date:   November 6, 2010

Time:  7:30am – 4:30pm

Where:  Indianapolis, Indiana at the downtown University Place Hotel

Register now!

This Event Has Been Approved for 7.5 Contact Hours

About Pearl IRB

Pearl IRB is an independent Institutional Review Board that provides comprehensive IRB services for 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 at www.pearlirb.com, call us at 317.278.4100, or email info@pearlirb.com.

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