Rethink, Reignite, and Reimagine Clinical Research

Real-world data (RWD) and real-world evidence (RWE) are playing increasingly important roles in healthcare and are making it possible for decision makers to gain insights and incorporate more data quickly into research decisions. Optimization of this data will enable researchers to design and conduct clinical trials more efficiently, both from a cost and timeline perspective. This webinar focuses on the significance of leveraging data management technology to increase collaboration amongst stakeholders and maximize the value derived from the data provided newer platforms.

Register Free: https://www.pharmexec.com/pe/rethink-reignite-reimagine

Event Overview:

Real-world data (RWD) and real-world evidence (RWE) are playing increasingly important roles in healthcare and are making it possible for decision makers to gain insights and incorporate more data quickly into research decisions. Optimization of this data will enable researchers to design and conduct clinical trials more efficiently, both from a cost and timeline perspective.

However, accessing and analyzing large amounts of data can be unwieldy and resource intensive. How do we ensure sponsors, sites, regulatory authorities, and study teams can efficiently and easily manage this wealth of new data to deliver actionable insights? And how can we streamline complex data sets into a single and actionable source of truth?

This webinar focuses on the significance of leveraging data management technology to increase collaboration amongst stakeholders and maximize the value derived from the data provided newer platforms.

Key Learning Objectives

• Opportunities and challenges stakeholders face when exploring RWD/RWE
• Best practices to produce robust and meaningful RWD/RWE that can be streamlined from complex data sets into a single and actionable source of truth
• How innovative data capture can be utilized to improve patient safety and clinical burden in clinical trial research

Who Should Attend

This webinar is applicable to:

• Sponsors, CROs, Clinical Researchers, Data Scientists, and Clinical Decision stakeholders whose roles may include:
  • Clinical development planning
  • Study design
  • Country and site identification, feasibility assessment, selection, and activation
  • Clinical data management, collection, and evaluation of trial metrics
  • Project management of studies, process optimization, and operational excellence
  • Management of patients and measurement of clinical outcomes
    

Full Agenda
Thursday, March 21st: 
11:00 am EDT Unlocking Potential and Navigating Limitations of Using Real-World Evidence in Safety
Martina Furegato, Associate Principal; Oracle Life Sciences
Robert Weber, Product Management Director; Oracle Life Sciences
Elise Berliner, Global Senior Principal of Real-World Evidence Strategy; Oracle Life Sciences


12:00 pm EDT Taming the Data Tsunami From Decentralized Clinical Trials and Real-World Data
David Blackman, Executive Director Digital Trials Strategy; Oracle Life Sciences


1:00 pm EDT Creating the Future in Clinical Research with CROs Using Real-World Data

Speakers:

Martina Furegato
Associate Principal
Oracle Life Sciences

Robert Weber
Product Management Director
Oracle Life Sciences

Elise Berliner
Global Senior Principal of Real-World Evidence Strategy
Oracle Life Sciences

David Blackman
Executive Director Digital Trials Strategy
Oracle Life Sciences

Register Free: https://www.pharmexec.com/pe/rethink-reignite-reimagine