Finding the Right Partner for Your Clinical Trial

This event is now available on demand.

Event Overview

Faced with an increasingly more competitive future, CROs are spearheading of adoption of modern clinical applications to increase efficiency, enhance collaboration, and improve clinical trial performance. Advances in clinical trial processes have arisen as a result of cross-company collaborations amongst CROs and various industry stakeholders – constrained by time and compelled by regulatory compliance – to support broader industry-wide adoption of innovations.

Learn more in this webinar about why CROs are advocating for operational shifts necessary to support the adoption of innovative solutions to capture data and the significance of partnering with a CRO who can support initiatives throughout the entire clinical trial continuum using innovative data capture methods and their knowledge to facilitate global submissions.

Key Learning Objectives

How CROs have leveraged innovation to help accelerate clinical trials.
The importance of a single data foundation in providing an open platform to support interoperability, delivering actionable insights while simplifying business optimization.
What it takes to operationalize decentralized clinical trial study designs with innovative data capture methods.
What it requires to have necessary oversight of global submissions to avoid incurring global study time penalties.

Who Should Attend

Life Sciences executives
Pharmacovigilance professionals
Sponsor and CRO roles responsible for:
- Clinical development planning
- Study design
- Country and site identification, feasibility assessment, selection, and activation
- Clinical data management, and collection and evaluation of trial metrics
- Project management of studies, process optimization, and operational excellence
- Global, EMEA and country project management of studies, process optimization, and operational excellence
- Country and site identification, selection, study package contracting, and site documentation
- EMA regulatory submissions
US Central IRB roles who are responsible for generating study content for IRB submission of global studies

Full Agenda

Thursday, May 9th:

10:00 am EDT Driving Your Organizations Success and Transformational Initiatives in Clinical Trials
Ryan Kennedy, Global VP, Product Strategy, Experience, and Enablement; Oracle
Sean Roy, Senior Consulting Practice Director; Oracle
Drew Zwiebel, Global Vice President, Alliances & Channels; Oracle
Raj Modi, Senior Director, Global Customer Centre of Excellence; Oracle

11:00 am EDT The Conundrum of Proliferating Data from Decentralized Clinical Trials
David Blackman, Executive Director Digital Trials Strategy; Oracle, and other non-Oracle speakers.

12:00 pm EDT How CROs Are Leveraging Innovation to Accelerate Clinical Trials
Non-Oracle speakers

1:00 pm EDT How EU 536/2014 Will Revolutionize Global Clinical Trials
Elvin Thalund, Director, Industry Strategy; Oracle, and other non-Oracle speakers

Featured Speakers