Now more than ever, the important work of this clinical research community requires collaboration and innovation. In its 14th year of fostering these goals, SCOPE Summit 2023 will take place February 6-9, 2023 in Orlando, FL at the Rosen Shingle Creek, over four stimulating days of in-depth discussions in 28 different conferences, 3 plenary keynote sessions, the 7th annual Participant Engagement Awards, special cross-department panels, the 2nd annual golf tournament, and the ever-popular interactive breakout discussions. The programming focuses on advances and innovative solutions in all aspects of clinical trial innovation, planning, management and operations. SCOPE 2022 attracted more than 2,300 leaders in clinical operations and research and all conference tracks will feature best practice case studies relevant to clinical operations experts and those new to the field.

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SCOPE Europe, hosted on 17-18 October 2023, in Barcelona, Spain, gathers clinical innovation leaders, clinical operations executives, and those responsible for the planning and management of clinical trials in Europe and the rest of the world. Building on the success of its long-running US-based counterpart, the 6th Annual SCOPE Europe: Summit for Clinical Ops Executives is a two-day executive conference serving clinical innovation leaders, clin ops execs, digital leaders, functional heads, category managers, and those responsible for the planning and management of clinical trials in Europe and the Rest of the World. This event brings together leaders from large, mid-sized, and small pharma, specialty pharma, biotech, CROs, vendor companies, and academic research centers who come together to share best practices and discuss the new era of decentralized, analytics-driven and patient-centric trials. The event features four conference tracks, shared plenary keynotes, interactive small breakout discussion groups, panels, networking and tapas, of course. Topics to be discussed include the digitalization of trials, decentralized/hybrid trial operations, adapting to COVID, protocol development, global site selection, feasibility, study start up, patient engagement, diversity/equity, enrollment planning, patient recruitment, patient retention, improving site-study activation and performance, new regulations and guidelines, Risk-Based Monitoring (RBM), clinical technology, big data and analytics, Real-World Data (RWD), Artificial Intelligence (AI), biomarker-driven trials, and improving overall quality and speed of clinical trials.

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