How Research Sites Can Win with Decentralized Trials – Part 1 – Remote Feasibility

The last twelve months have been a year of unprecedented and transformative adaptation in clinical research. In this 7-part webinar series, industry experts share their collective reflection on decentralized trial modalities and their role in advancing the research of tomorrow. From e-Consent forms to remote patient monitoring, technology will continue to support this process. Sourcing and vetting new vendors and staying on budget are among the challenges ahead, but one overarching question remains – how can research sites win with de-centralized trials?

From the lifecycle of a remote clinical trial to effective feasibility and planning, patient recruitment, regulatory compliance, and continuity of operations, this is one energetic and spirited conversation you won’t want to miss.

Topics covered over the course of 7 sessions include:

• Part 1 – Remote Feasibility & Planning
• Part 2 – Patient Recruitment
• Part 3 – Remote Consenting
• Part 4 – QA/ QC Remote Monitoring
• Part 5  – Regulatory Compliance
• Part 6  – Continuity of Operations
• Part 7 – Leadership & Technology

Panelists

Raymond Nomizu, CEO & co-founder, Clinical Research IO (CRIO) – a site-centered eSource and CTMS solution

Edye T. Edens, Senior Research Compliance Consultant, First Class Solutions

Daniel Perez, COO, MACRO Trials – a Site Optimization Organization (SOO)

Maya Zlatanova, CEO, TrialHub

And this is only the beginning. Up next? How Research Sites Can Win with De-centralized Trials – Part 2 – Patient Recruitment.

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