While the digital transformation of clinical trials has made tremendous strides in recent years, the plethora of new technologies is overwhelming sites. To run one clinical trial, the investigative site team can use up to 15 different systems (e.g. EDC, EHR/EMR, payments, CTMS, radiology, technology vendors, etc.)

In this webcast, featured speakers from GSK, Medable, and Alcanza Research will thoroughly explore sites' experiences of digital/hybrid trials. They'll discuss the importance, and benefits, of implementing a change management strategy coupled with a unified digital trial platform that streamlines eConsent, eCOA, sensors and integration workflows into a single end-to-end experience.

Key Learning Objectives

• Site pain points associated with digital trials (lack of flexibility, autonomy, and budget)
• Guidelines to ensure the optimal combination of technologies for sites
• Effective change management tactics to make sites comfortable with new technologies
• A case study of effective digital trial implementation to maximize site productivity
• Sponsor of Choice: Empowering Sites with a Voice

Who Should Attend

• Large Pharma, Biotechs, & CROs
• Clinical IT, Business IT, Clinical Operations/Research/Development, Study Management, Therapeutic Area Leads, Portfolio Leads, Innovation Leads, Procurement Leads, Science Teams, Medical Affairs, Data Management/Analysis/Process, Regulatory Affairs Heads, QA/QC, R&D, Chief Medical/Scientific Officers, Patient-centric Titles