In today’s complex clinical trial landscape, traditional site selection methods based solely on historical experience are no longer sufficient.
Sponsors face increasing challenges in global trial execution, from navigating competitive environments to managing variable site performance.
This webinar explores how integrating independent, holistic data with precision feasibility strategies can transform site enablement and patient recruitment, unlocking new levels of trial success.
Site enablement begins with understanding not just which sites have performed well in the past, but which are truly positioned to engage and recruit the right patients.
By leveraging global insights into patient journeys and site engagement patterns, sponsors can identify high-performing sites and uncover untapped opportunities.
This includes mapping patient pockets across geographies and understanding how patients interact with healthcare providers at various sites, which is critical for identifying diverse populations and non-investigator physicians who have access to eligible patients.
Patient recruitment driven by tokenized and longitudinal real-world data (RWD) enables unrivaled precision in targeting. This approach allows sponsors to pinpoint where patients are, when they appear and how best to reach them. But precision alone is not enough. The combination of data-driven insights with last-mile services, which directly engage patients and facilitate trial participation, is needed.
Attendees will gain a comprehensive view of how patient insights and feasibility capabilities support global trial planning, from identifying optimal sites to deploying recruitment strategies that scale. The featured speakers will highlight how independent data refreshes assumptions, validates site potential and supports confident decision-making. They will also showcase how precision targeting and patient engagement services converge to deliver measurable outcomes.
Register for this webinar to explore actionable strategies that improve patient recruitment performance, optimize site selection and engage the right patients.
Speakers
Skye Hodson, PhD, VP Clinical Solutions, Citeline
Skye is a Biochemist with over 10 years of life sciences CRO and CCO experience, delivering tangible business outcomes across strategy, product development, clinical operations, commercialization and growth. He focuses on leveraging enabling technologies to accelerate the development of new medicines, having seen firsthand how data-driven insights and advanced analytics/AI can unlock real value for patients and companies. He is passionate about disrupting the status quo and advancing holistic health agendas, engaging with the community as a speaker, mentor and advocate for innovation in life sciences.
Lindsay Stahl, VP, Global Head of Patient Engagement and Recruitment, Citeline
As Vice President, Global Head of PE&R, Lindsay Stahl leads Citeline’s Patient Engagement and Recruitment portfolio and is responsible for helping guide, grow and deliver on our Patient Engagement and Recruitment solutions. She has over 15 years of experience in scientific and clinical research & development, partnership development and real-world data strategy and solutioning for clinical investigation, across academic, biotech, data vendor and pharmaceutical spaces.
Who Should Attend?
This webinar will appeal to professionals in the following roles or areas of expertise:
- Clinical Operations/Clinical Development
- Clinical Research/Clinical Strategy
- Study Management/Patient Recruitment
- Patient and Site Engagement Leads
- Feasibility Leads
What You Will Learn
Attendees will learn how to:
- Accelerate trial enablement by selecting sites proven to perform and ready to engage patients
- Reach the right patients faster with precision insights into who they are, where they are and when they’re ready
- Boost recruitment results with next-generation, outcome-based last-mile engagement services
Xtalks Partner
Citeline
Citeline, a Norstella company, powers a full suite of complementary business intelligence offerings to meet the evolving needs of life science professionals to accelerate the connection of treatments to patients and patients to treatments. These patient-focused solutions and services deliver and analyze data used to drive clinical, commercial and regulatory-related decisions and create real-world opportunities for growth.
Citeline’s global teams of analysts, journalists and consultants keep their fingers on the pulse of the pharmaceutical, biomedical and medtech industries, covering it all with expert insights: key diseases, clinical trials, drug R&D and approvals and market forecasts. For more information on one of the world’s most trusted health science partners, visit Citeline.
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