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COVID-19 amplified burdens for sponsors, CROs and sites, but especially for participants who faced increased costs and questions around getting to the clinic.  
 
The clinical trial industry responded swiftly, adapting to the global shutdown with bold new ways to conduct trials. Automation has been key to success.
 
In fact, 84% of sponsors and CROs are actively seeking to increase the use of technology to better support decentralized trials. 
 
When the catalyst of the pandemic wanes, we risk losing the progress we have made unless we collectively refuse to go back to the way things were before - and instead dedicate ourselves to implementing even more advancements and innovations that we've only dreamed of so far.  

Attend this webinar to discover:

  • Why eClinical technology tools are crucial to delivering on patient and site centricity
  • How integraing eCOA and payments can increase retention and improve compliance
  • What the considerations are for global implementation and localized requirements

Start planning for the future of clinical trial conduct now to ensure that trials remain efficient, fast, reliable, and trusted. There is #NoGoingBack.

Speakers:

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Kyle Cunningham

Chief Product Officer

Greenphire

As Chief Product Officer, Kyle leads the strategic direction of Greenphire’s solution development, ensuring that our product innovation roadmap is constantly evolving to solve relevant healthcare industry problems - ultimately creating value for sponsors, CROs, clinical research sites and study participants.  

Kyle has two decades of experience across multiple industries and in a variety of roles spanning innovation, operations management and client experience.  Prior to joining Greenphire, Kyle worked for SEI Investments (Europe) where he managed product and service innovation for global asset management.  

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Jill Platko MD

Senior Scientific Officer

Signant Health

At Signant Health, Dr. Jill Platko provides scientific guidance in both the presales process and for projects. This includes the review of clinical trial protocols, to determine ePRO data collection design. Her role is to ensure that CRF’s technology meets the scientific requirements of clinical trial sponsors.

Moderated by

Maire Gerrard

Custom Content Writer

Informa Pharma Intelligence

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