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Home >

Best Practices for Enabling Accelerated and Equitable Global Drug Development


$79.00
 (Non-Member Price)
$0.00 (SCRS members – Included as member benefit, no additional cost)

Not an SCRS member? Join now to attend this webinar at no additional cost.


Date and Time: August 2, 2022 @ 12:00 PM ET


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


Presenter:
Adam Wyckoff, Director of Product Management, Clinical Trials, H1


Description:

In this informative discussion, we’ll look at the narrative and pivot of clinical trials and a much needed industry focus on diversity and equity since COVID-19. We’ll share real-world examples of how one top pharmaceutical company sought opportunities to work with diverse patient populations using clinical intelligence covering HCPs and investigators, institutions and sites, therapeutic areas, patient populations, and sponsors. 


From exploring potential investigators for decentralized trials to protocol development and performance analysis, learn how to use data-driven decision making in clinical trial development, operations, feasibility, and analytics that yield successful and insightful results for a more inclusive trial. 

In this webinar you'll learn: 

    1. 1. Perspective best practices for data driven decision making to enhance diversity in investigator profiles and patient populations. 
    2. 2. How to find and understand diverse key opinion leaders (KOLs) during product development
    3. 3. Which key D&I data elements are critical to a sound strategy
    4. 4. How to sources the data for sustainable, long-term success and understand principal investigator profiles and clinical trial sites for access expansion to therapeutic options for patients. 


Speaker Bios: 

Adam Wyckoff, Director of Product Management, Clinical Trials, H1

Adam Wyckoff is an experienced product leader who specializes in driving vision and roadmap for healthcare businesses, including strategy, sales enablement, product design and development.  He focuses on collaboration between customer and company, with cross-functional partners to deliver successful results. He has extensive experience in health tech, pharma, and healthcare, specifically in clinical trials and biomarker testing insights. In his role at H1, Adam works with product engineering, sales and data teams to build out strategy and vision for the H1 Trial Landscape product and to ensure H1 is delivering full value to customers. 

About H1:

H1 is the connecting force for global HCP, clinical, scientific and research information. The H1 Connect platform democratizes access to HCP knowledge and groundbreaking insights for life sciences, academic medical institutions, health systems, and payors. H1 Connect fuels a robust product that helps customers discover and engage industry experts, drive equitable research, access groundbreaking science, and accelerate commercial success with the most robust and accurate healthcare professional data. Learn more at h1.co.


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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To obtain your Contact Hours for this webinar:

  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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