Navigating Healthcare with Patients at the Center

This event is now available on demand.

Event Overview

In the realm of healthcare, patients are now more involved in their own care, with easy access to information through the internet and the use of new technologies that empower them to generate and share data. Patients are not only the beneficiaries of scientific knowledge but are creators of scientific knowledge. As a result, (bio)pharma companies are recognizing the potential benefits of engaging with highly motivated patients and patient organizations. This approach not only reduces costs but also enhances the success of clinical trials.

Join this webinar to learn more about including patients as partners in clinical research and utilizing technology to collect relevant patient-centric, real-world data to improve the design and outcomes of clinical trial research studies, advocate for patient equity, and advance scientific and drug discovery.

Key Learning Objectives

Understand the impact of trial design on participants and why a patient-centric approach can lead to more successful clinical trials.
Become familiar with FAIR and CARE principles and learn how to ensure proper data standards across many data constituents, collaborations, and frameworks.
Understand how diverse and inclusive patient recruitment could serve as key access enablers for patients to receive clinical research as a care option.
Learn how to implement patient assessments in remote settings and ensure results are robust and meaningful.
Hear perspective on what to expect from future trial models based on current trends in the industry.

Who Should Attend

Clinical researchers, academic researchers, data scientists, patient engagement leads, and clinical decision teams responsible for:
- Research data computing and planning
- Clinical development planning and study design
- Management of patients and measurement of clinical outcomes
- Clinical data management, collecting and evaluating trial metrics.
- Project management of studies, process optimization, and operational excellence

Sponsors and those with CRO roles who are responsible for:
- Clinical development planning
- Study design
- Country and site identification, feasibility assessment, selection, and activation
- Clinical data management, collecting and evaluating trial metrics
- Project management of studies, process optimization, and operational excellence

Full Agenda

Thursday, April 18th:

10:00 am EDT Addressing Diversity in Patient Recruitment for Clinical Research
Katherine Vandebelt, Global Vice President, Clinical Innovation; Oracle, and other non-Oracle speakers.

11:00 am EDT Addressing Enrollment and Trial Inefficiencies With Patients as Partners
Rebecca Nash, Principal, Real-World Evidence; Oracle
Kathy Beusterien, Senior Research Scientist; Oracle, and other non-Oracle speakers.

12:00 pm EDT Do Decentralized Trials Still Offer Clinical Precision in Challenging Patient Populations?
Gillian Worman, Director, Product Strategy; Oracle
David Blackman, Executive Director, Digital Trials Strategy; Oracle, and other non-Oracle speakers.

1:00 pm EDT Advancing Drug Discovery and Treatment Options with Patients and Citizen Science
Amy Sorrells, Senior Director; Oracle, and other non-Oracle speakers.

2:00 pm EDT Accelerating Precision Oncology with Artificial Intelligence
Elise Berliner, Global Senior Principal of Real-World Evidence Strategy; Oracle, and other non-Oracle speakers.

Featured Speakers