How EQRx Improved Site Engagement During Study Start-Up

Life Sciences, Clinical Trials,
  • Thursday, January 13, 2022 | 11am EST (NA) / 4pm GMT (UK) / 5pm CET (EU-Central)
  • 60 min

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

http://Lauren%20Kingston,%20EQRx

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.

Message Presenter
http://Anusha%20Shetty,%20Veeva%20Systems

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.

Message Presenter

Who Should Attend?

Senior professionals, including:

  • Head of Study Start-Up
  • VP of Site Operations
  • Director of Clinical Trials
  • Study Start-Up Specialist
  • Clinical Trial Specialist
  • Clinical Trial Associate (CTA)/Clinical Research Associate (CRA)
  • Study Manager
  • Site Activation Lead
  • Feasibility Manager
  • Head of Site Management

What You Will Learn

In this webinar, participants will 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

Xtalks Partner

Veeva

Veeva’s industry cloud solutions provide data, software, services, and an extensive ecosystem of partners to support your most critical functions from R&D through commercial. Veeva Vault Clinical Data Management Suite offers EDC, data cleaning, coding, and review in a single unified suite. You can manage study build through execution and gain a complete and concurrent view of all clinical data within a trial. Vault CDMS accelerates study timelines by reinventing traditional data management systems and processes. Learn more at veeva.com/cdms

Media Partner

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