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New Research: Patient Data Collection Concerns in Pandemic Environment

New Research: Patient Data Collection Concerns in Pandemic Environment

OVERVIEW 

The COVID-19 pandemic has - without warning - turned clinical operations on its head, forcing the clinical research industry to re-evaluate how to manage clinical trials. In an instant, physical access to patients across the globe ceased to be an option and the impact on data collection and patient monitoring has been significant.

In this new environment, many organizations have accelerated their plans to shift to a decentralized clinical trial model. With this transition comes many benefits and challenges, and begs the question: are clinical development organizations prepared for this paradigm shift?

Oracle Health Sciences, in partnership with Informa Research sought to gather insight on the impact of the Covid-19 pandemic on clinical data collection and clinical operations by conducting an industry-wide survey. The survey reveals the depth of the pandemic’s impact on clinical trials and reveals industry leaders’ future predictions for clinical development beyond 2020.

WHAT YOU'LL LEARN 

  • Hear research results from a recent global, industry-wide survey on data collection in the pandemic environment.
  • Learn how your peers are adapting to clinical data collection in a pandemic situation.
  • Understand the regulatory challenges and concerns regarding remote data collection.
  • Learn ways for clinical operation readiness in this new world.

WHO SHOULD ATTEND

All levels are welcome to join as this will be a research-data driven discussion, with time for Q&A. Typically, we see Director and above from Clinical Operations, Data Management, and Innovations, and due to a focus on regulations, Regulatory Heads.

WHAT ARE THE BENEFITS 

Participants will learn how their peers are handling data collection in the pandemic environment, specifically, what their concerns are and the tactics they are using to manage it.

MEET THE PRESENTERS

James Streeter, Global Vice President, Life Sciences Product Strategy, Oracle Health Sciences.

As the global head of life sciences product strategy for Oracle, James Streeter collaborates closely with Oracle customers, regulatory agencies, analysts, and industry thought leaders to develop and help execute the overall business and product strategy for Oracle Health Sciences. He previously held leadership roles at PPD in both operations, as the Global Head of Global Clinical Technical Operations and EDC and recently in IT, as Global Head of Systems Development, Business Operations Teams, and eClinical Strategy and Innovation.

James has 29 years of data acquisition and analysis experience utilizing computerized systems and has focused on eClinical systems and processes for trials for the last 19 years. James’ experience includes implementing end to end eClinical Solutions and processes across all therapeutic areas and all phases of studies.

James’ early experience in eClinical was gained at Pfizer Inc., where he was Senior Director of Global Clinical Data Services, heading the global data acquisition department for the company’s global research and development organization. Prior to joining Pfizer, he was a Senior Hardware, Software and Systems Engineer for the U.S. Navy Underwater Sound Laboratory with a focus in data acquisition and analysis.

Kristin Letourneau, PhD - Director of Market Research, Informa Engage

With over 25 years of research experience in both corporate and academic settings, Kristin Letourneau currently serves as the Director of Market Research for Informa Engage. Kristin earned her PhD in Social Psychology with a concentration in Quantitative Methods from the University of Kansas in 2000. Her work has been published in several B2B publications over the years, as well as the academic journals Group Dynamics and European Journal of Social Psychology.


WEBINAR REGISTRATION

Group Registration Policy: Any group registration allows up to 10 people to attend the webinar and to complete the webinar assessment. Credits will be granted on an individual basis upon successful completion of the assessment by the registered participants.

Refund Policy: Participants will receive a full refund if notice is provided in writing via post or email one week prior to the webinar date. If cancellation occurs within the week prior the webinar, participants will be allowed to apply 50% of the webinar fee to the next offering of the same webinar. No refunds will be offered after that time.

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