Improving Your Site Feasibility

A WCG | CenterWatch FREE Webinar
Tuesday, March 27, 2018 • 1:30 p.m. - 2:30 p.m. EDT

Site selection is essential to your clinical trials, so you must be laser-focused on site feasibility.

Think about it. Site selection is the introduction — a first date — between the site and a sponsor or CRO. And then there’s a determination of whether the relationship is going to move forward. What are the study design and deadline assumptions? Like any relationship, how do you determine if this is the right one for you?

Exactly how do you go about making perhaps the most difficult decision in the clinical trials process when it impacts everything in the trial itself? How much time and analysis should you spend on this critical game-changer?

As a sponsor or CRO, you simply cannot have a flawed feasibility process. You cannot continue to blast out cumbersome, repetitive and lengthy questionnaires with extraneous questions, bombarding a potential site with even more e-mail solicitations.

Stop the madness. Learn how to make your questionnaires more succinct, your data actionable, and your study more appealing to prospective sites. Bottom line: Be more productive. Increase your response rates.

The good news: In just 60 minutes, from the comfort of your own office, you can take a practical, insightful dive into this quagmire and emerge with a fuller understanding of how to determine site feasibility. Don’t spend thousands more dollars on attorneys and consultants. In fact, don’t spend any money at all because this webinar is free. Simply save this date — March  27, 2018 — to hear one of the leading authorities on the site feasibility selection to explain how to:

  • Pre-identify the most likely high-performing sites based on available historical performance data;
  • Provide advice for tightening up feasibility questionnaires to reduce site burdens;
  • Give real-world examples of do’s and don’ts in questionnaire development and how to do it more effectively;
  • Offer insights into response data review and how to handle discrepancies;
  • And much more!

As the industry trends toward doing more with less while expanding globally, it is more important than ever to ensure companies nail the feasibility aspect of trial management. As a sponsor or CRO, you can’t afford to waste time and money on underperforming sites or miss projected timelines in this competitive landscape.

Really, don’t you want to make the site feasibility selection process more predictable, less costly, and far, far more productive?

Your presenter, Wes Martz is an Associate Director in ePharmaSolutions’s Clinical Services division, specializing in feasibility and patient recruitment. Martz has helped dozens of clients with protocol and site feasibility, and he can support your organization too.

Take advantage of this free, practical presentation to learn the nuances of site feasibility selection. Sign up now.

Who Will Benefit

This session is perfectly suited to those dealing with site selection feasibility, including professionals holding these job titles:

  • Director/Associate Director Clinical Research
  • Feasibility Specialists
  • Study Managers

Sign Up for FREE Below

Meet Your Presenter


Wes Martz

Associate Director, ePharmaSolutions’s Clinical Services division

Wes Martz is Associate Director in ePharmaSolutions’s Clinical Services division, specializing in feasibility and patient recruitment for almost 15 years. Martz has helped more than 50 clients with protocol and site feasibility and patient recruitment campaigns. Recently, Martz has been instrumental in overhauling a company’s site feasibility process leading, to increased response rates, improved data quality and presentation, and global decision-making transparency.