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Patient Engagement & Recruitment ON-DEMAND WEBINAR

Boost Participant Recruitment with Precision Feasibility and RWD

Watch on-demand this webinar to explore actionable strategies that improve patient recruitment performance, optimize site selection, and engage the right patients.

Citeline and XTalks side by side.

About this webinar

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 unrivalled 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.


Featured speakers

Headshot of Lindsay Stahl.

Lindsay Stahl

VP, Global Head of Patient Engagement and Recruitment, Citeline

Citelineの患者エンゲージメントおよびリクルートメント部門統括として、当社のソリューションの方向性策定、成長戦略の推進、提供価値の最大化を担うLindsayは、科学・臨床研究開発、ならびに臨床試験におけるリアルワールドデータ戦略およびソリューション設計において、15年以上の経験を有しています。

コロンビア大学で疫学の修士号(MS)、ニューヨーク市立大学ハンター校で生物心理学の修士号(MA)、ロードアイランド大学で心理学の学士号(BA)を取得。

Headshot of Lindsay Stahl.

Lindsay Stahl

VP, Global Head of Patient Engagement and Recruitment, Citeline

Citelineの患者エンゲージメントおよびリクルートメント部門統括として、当社のソリューションの方向性策定、成長戦略の推進、提供価値の最大化を担うLindsayは、科学・臨床研究開発、ならびに臨床試験におけるリアルワールドデータ戦略およびソリューション設計において、15年以上の経験を有しています。

コロンビア大学で疫学の修士号(MS)、ニューヨーク市立大学ハンター校で生物心理学の修士号(MA)、ロードアイランド大学で心理学の学士号(BA)を取得。

Join us to discover how precision feasibility and RWD are transforming clinical trials
What you'll learn
  • What’s Changing: Gain a clear understanding of the new ICH GCP E6(R3) guidelines and why they matter
  • Who’s Affected: See how sponsors, CROs, sites, ethics boards and patients are impacted
  • What You Need to Do: Explore practical approaches to more intelligent risk management and data governance to stay compliant
  • What’s The Opportunity: Discover how to turn regulatory change into strategic advantage and growth