How EQRx Improved Site Engagement During Study Start-Up

Study start-up is one of the most complex and heavily regulated components of a clinical trial launch. This period involves multiple handoffs and stakeholders, often working in silos due to disconnected Excel trackers and disparate technology. Sponsors and contract research organizations (CROs) need to streamline key processes, such as essential document collection, and automate data flows between study partners to greenlight research sites as quickly as possible and maximize enrollment timelines.

In this webinar, fast-growing biotech EQRx will share their innovative technology and business process approach that transforms how they exchange documents and information with their sites to improve start-up timelines and strengthen site relationships.

Register for this webinar to learn:

• The key drivers to look for in study start-up technology
• Tips to improve the quality of engagement with sites
• Implementation strategies to build a scalable foundation for efficient cross-functional collaboration

Speakers

Lauren Kingston, Director, Clinical Trial Initiation, EQRx

Lauren has over 15 years’ experience in clinical operations working in the pharmaceutical and CRO sectors with a primary concentration in global study start-up. She has held leadership positions with two large CROs and has extensive experience with driving initiatives that optimize global processes, people and technology. Lauren is passionate about leveraging analytics to facilitate data-driven decision-making to improve operational performance.

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Anusha Shetty, Director, Clinical Strategy, Vault Study Startup, Veeva Systems

Anusha is the strategist and market owner for Vault Study Startup. She is responsible for growing and sustaining the market for the Vault Study Startup product. Anusha has over 13 years of experience in technology and consulting and has spent most of her career implementing life sciences technologies with a focus on study start-up for the last seven years.

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