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

Presented By

James Wurdeman
SVP Strategy and Innovation

Ian Shafer

Dana Glisson
Global Head of Site Readiness and Regulatory

Erin Williams
VP, Contracts and Regulatory
Velocity Clinical Research

Laura Edgerton
Associate Director, SSU Namer
Syneos Health
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Who should watch?

This content applies to research professionals representing sponsors and CROs who are involved in the planning, development, and execution of clinical trials.

CE Credits

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.

This event may qualify for continuing education (CE) credits. Please check with your professional organization(s) to determine whether the event meets their CE eligibility requirements.

Certificate of Attendance

After watching this webinar in its entirety and completing the webinar survey, 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, watch the webinar in its entirety, and complete the webinar survey. Visit our Webinar Help page for more information on certificates of attendance.

DATE: June 17, 2021
Time: 1 pm ET | 10 am PT
Duration: 1 hour

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