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Simple Ways to Uncover Research Compliance Blind Spots


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Date and Time: April 26, 2022 @ 12:00 PM ET


Contact Hours: One contact hour will be issued.
Contact Hours are not available for archived webinars.


Presenters:

David Staley, MA, Associate Director, Institutional Research Center of Excellence, Advarra
Draco Forte, M.Ed., CHRC, Associate Director, Institutional Research Center of Excellence, Advarra

Description:

Research compliance professionals routinely confront complex and uncertain situations. Questions often arise about improving informed consent compliance, addressing weightier compliance risks throughout institutions, or increasing the chances a new compliance initiative might succeed. But the most challenging of compliance entanglements are all too often unexpected and imperceptible: research compliance professionals haven’t realized they should be paying attention, or why they need to. The reason? Blind spots. In this webinar, Draco Forte and David Staley of Advarra offer three strategies to check and reduce blind spots regularly to improve compliance oversight.
    1. 1. Outmaneuver complex situations by learning to identify blind spots in areas of research compliance
    2. 2. Study a scenario and use prospective hindsight to navigate potential pitfalls in best practice thinking and avoid jumping prematurely to noncompliance
    3. 3. Identify ways to test implicit compliance assumptions


Speaker Bios:

David Staley, MA

Associate Director, Institutional Research Center of Excellence

Advarra


Accomplished leader, writer, and public speaker with eighteen years of experience working in human subjects research protection programs and research operations, more than ten years of which leading in a dynamic research enterprise.




Draco Forte, M.Ed., CHRC

Associate Director, Institutional Research Center of Excellence

Advarra

Specialties: Expertise in healthcare, program implementation and management, process improvement, ethical conduct of clinical research (IRB, conflicts of interest), good clinical practices, clinical research regulations (OHRP, FDA, PHS, CMS) and clinical research administration, clinical research billing. Certification in Healthcare Research Compliance (CHRC) from The Compliance Certification Board.




Society for Clinical Research Sites, Inc. is accredited as a provider of continuing nursing education by the American Nurses Credentialing Center’s Commission on Accreditation.

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  1. The webinar must be watched in its entirety.
  2. The post webinar survey immediately following this webinar must be completed in its entirety.
  3. Your contact hour certificate will be sent to you within 30 days of you viewing this webinar.
  4. The contact hour certificate will be sent to the email address provided when you registered.

Planners, presenters, faculty, authors, and content reviewers do not have any relevant financial relationships with any commercial interest.

This webinar does not imply any endorsement of products or services by the Society for Clinical Research Sites or ANCC.

The materials and recording of this webinar will be available for one year as an archive, but will not award any contact hours.


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