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Leveraging RBQM Technology to Enable Sponsor-Level Clinical Trial Oversight

This event is now available on demand. 

Register for the event to gain free access to all sessions.    
Event overview

Oversight of a clinical trial is the regulatory responsibility of the Sponsor, but even with technological advances, data transparency can be limited with outsourced trials. So how can Sponsors meet the regulatory criteria for oversight with such limited data access?
 
By providing a holistic view of trial data, RBQM technology is one way that Sponsors can observe and confirm the highest quality of data while minimizing the risk of unexpected issues or delays. The resulting benefits include improving the efficiency, reliability, and effectiveness of clinical research programs.

Three key take-aways

Join this session to discuss:
  • The varied definition of oversight between Sponsors and CROs
  • How a risk-based quality management approach facilitates consistent and near real-time trial oversight
  • How RBQM technology can enable trial oversight




Rachael Geedey
Associate Director, RBQM Technology
IQVIA Technologies

Rachael Geedey brings expertise in technology training, adoption and implementation across various clinical trial platforms. She is passionate about people, process and technology and has extensive operational experience supporting study teams in the use of RBQM technology. Rachael is currently an Associate Director supporting IQVIA’s Risk Based Quality Management SaaS Solution.

Email: rachael.geedey@iqvia.com
LinkedIn: https://www.linkedin.com/in/geedey/
 

  
 
Gayle Hamilton 
Director, RBQM Technology 
IQVIA Technologies

Gayle Hamilton is an experienced risk-based management project advisor and project lead with a strong background in clinical operations and project management. She has supported study trial teams and IT development in RBQM implementation across all phases and therapeutic areas, driving the development of processes, tools, and systems. Gayle is also experienced in assuring high-quality business performance of clinical operations within global projects.

 Email: gayle.hamilton@iqvia.com
LinkedIn: https://www.linkedin.com/in/gayle-hamilton-74ab3310/
 
For any technical questions please contact Jordan Ramesh: jramesh@mjhlifesciences.com