SCDM 2025 Annual Conference

Hey Data, Where To Next? – The Festival of Opportunity

Join Medidata at SCDM 2025 in Baltimore, 27-30 September 2025, to advance clinical data management (CDM) excellence. Discover how AI is transforming study build and data review, and explore advancements in Risk-Based Quality Management (RBQM) and patient centricity. Attend our showcases and visit booth 403 to see how the Medidata Data Experience simplifies and accelerates data workflows from protocol to database lock.

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Thought Leadership and Solution Presentations

Saturday, September 27 @ 10:30 A.M. – 6:30 P.M.

Leadership Forum

Session Chair: Wayne Walker, SVP, Data Experience, Medidata;
Sunday, September 28 @ 3:20 P.M.

Implementing a Clinical Data Platform to Drive Transformation to Clinical Data Science

Speaker: Olgica Klindworth, VP R&D, Clinical Data Studio, Medidata;  
Sunday, September 28 @ 4:15 P.M.

From LLMs to SLMs: Will Clinical Data Science redefine Clinical Trial Execution?

Speaker: Jia Chen, Senior Director, AI Product Strategy & Growth, Medidata;  
Monday, September 29 @ 12:25 P.M.

One-click Study Build: How Medidata is Transforming EDC Design with AI

Speaker: Marco Amorim, Senior Director, Product Management, Medidata;
Monday, September 29 @ 3:00 P.M.

Navigating and Leading the Next Industry Revolution in Clinical Data Management

Speaker: Wayne Walker, SVP, Data Experience, Medidata;
Monday, September 29 @ 3:05 P.M.

From Data to Empowerment: Innovating CDM Through Patient-Centricity

Speaker: Karen Wood, Patient Insights and Advocacy, Medidata;
Monday, September 29 @ 5:15 P.M.

Practical Use (s) of AI for EDC Study Design and Build

Session Chair: Michael Barrera, Senior Director, Product Management, Data Experience, Medidata; Speaker: Marco Amorim, Senior Director, Product Management, Medidata;
Tuesday, September 30 @ 10:30 A.M.

Is it Time to Shift Gears in RBQM Implementation? – Arrival of RBQM 3.0

Speaker: Olgica Klindworth, VP R&D, Clinical Data Studio, Medidata;
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The Medidata Experiences

The life sciences industry is moving away from fragmented, standalone tools and embracing integrated, platform-based solutions. Sponsors, CROs, and sites increasingly demand end-to-end workflows connecting all clinical trial aspects. The Medidata Patient, Data, and Study Experiences, powered by automation and AI, improve patient engagement through digital technologies, enhance data quality with actionable insights, and optimize study design with predictive analytics.

Data Experience

The Medidata Data Experience connects every part of the clinical data process. From study build to data capture, database lock, and regulatory submission, it leverages built-in AI and automation to simplify workflows, reduce manual effort, improve data quality, and shorten trial timelines—turning raw data into real insights faster.

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Patient Experience

The Medidata Patient Experience provides an end to end technology solution for every stage of the clinical trial journey. From patient recruitment to study completion, Medidata’s unified platform centralizes capabilities in one patient portal, easing the patient burden and streamlining site workflows. Successful trials begin and end with empowered patients and sites.
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Study Experience

The Medidata Study Experience accelerates clinical trial design and management by seamlessly connecting workflows, data, and teams. Powered by AI and advanced analytics, it streamlines critical activities—like protocol design, site feasibility, budgeting, and trial execution—while delivering actionable insights that boost confidence, eliminate redundancies, and keep operations on track.
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