On-demand Webinar

Reducing Site Burden Throughout Study Startup

A key challenge to successful, timely study startup is the required coordination across multiple research stakeholders and the technology they rely on.

Being “site-centric” is being conscious of and committed to addressing the challenges preventing clinical trial sites from delivering the best possible experience for trial participants, and the best possible results for contract research organizations (CROs) and sponsors.

James Wurdeman, SVP Product Strategy and Innovation, hosts a panel of industry peers and experts from organizations including Syneos Health, Fortrea, Velocity, and PwC to learn strategies to:

  • Address timely challenges in study startup impacting sites, sponsors, and CROs
  • Review feedback from real sites on how to improve key workflows
  • Discuss use cases from industry peers on how they’ve reduced site burden and improved their site relationships
  • Learn strategies to improve budget negotiation, document management, site training, and more to implement at your organization

James Wurdeman

Advarra

SVP Strategy and Innovation

Ian Shafer

PwC

Partner

Dana Glisson

Fortrea

Global Head of Site Readiness and Regulatory

Erin Williams

Velocity Clinical Research

VP, Contracts and Regulatory

Laura Edgerton

Syneos Health

Associate Director, SSU Namer

Attendance at this session has been approved for 1.00 contact hour of research specific continuing education on applications for Maintenance of ACRP’s CCRC®, CCRA®, CPI®, or ACRP-CP® certification designations.

Provider approved by the California Board of Registered Nursing, Provider Number 17600, for 1 contact hour. This documentation must be retained by the licensee for a period of 4 years after the course concludes.

The Society of Clinical Research Associates (SOCRA – www.SOCRA.org) accepts documentation of candidate participation in continuing education programs for recertification if the program is applicable to clinical research regulations, operations or management, or to the candidate’s clinical research therapeutic area. This program offers 1 hour of CE credit.

If you would like to obtain CE credits for a different credential, please check with your professional organization to determine if our webinars meet their continuing education requirements.

There is no longer a survey component to the webinar. After watching this webinar in its entirety, you will receive a certificate of attendance. This certificate will be emailed to you within one business day of watching the webinar.

Please note that if your organization has other staff members who wish to get a certificate of attendance, each person must register and watch the webinar in its entirety. Visit our Webinar Help page for more information on certificates of attendance.

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