Study startup remains the most expensive and least improved phase of the clinical trial lifecycle. According to Tufts CSDD, site contract negotiations average 230 days, new sites take 36 weeks from first contact to first patient enrolled, and Phase III trials cost $55,716 for every day of delay. For small-to-mid biotech sponsors running two to five concurrent trials, these delays don’t just erode budgets – they threaten the survival of the program.
Yet the industry has entered 2026 at an inflection point. Agentic AI – autonomous AI agents that can reason, act, and adapt across clinical workflows – is now being deployed against study startup bottlenecks with measurable results. From automated database builds to intelligent site activation sequencing, these AI agents are compressing timelines that have remained stubbornly static for over a decade.
In this webinar, we unpack the anatomy of study startup delays, quantify the true cost of inaction using industry benchmarking data, and demonstrate how agentic AI is being applied to compress the study build-to-site activation timeline. We will walk through real-world application scenarios showing how AI agents automate protocol-to-database translation, accelerate site feasibility and selection, streamline regulatory document preparation, and enable parallel rather than sequential activation workflows.
Attendees will leave with a clear understanding of where their study startup process is leaking time and money, which AI-addressable bottlenecks offer the fastest payback, and a practical framework for evaluating agentic AI solutions against their operational reality.
This session is designed for PI’s, site leaders, clinical operations leaders, biotech executives, and CRO decision-makers who are past the “what is AI” stage and are looking for evidence-based, implementation-ready approaches to their most persistent operational challenge.
Register now to learn how leading clinical teams are applying Agentic AI to reduce delays, improve efficiency, and accelerate study startup timelines.
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Principal Investigator, Flourish Research
Dr. Rachna Saralkar is a double board-certified physician and Principal Investigator at Flourish Research, specializing in psychiatry, clinical informatics, and the application of AI in healthcare. She brings deep expertise at the intersection of clinical research, digital health, and emerging technologies, with a focus on advancing more efficient and patient-centered clinical development. Previously, she served as Medical Product Director at Deliberate AI, where she led the development of AI-enabled solutions for mental healthcare. She has also advised several early-stage health technology startups as a fractional Chief Medical Officer. Dr. Saralkar completed her psychiatry residency at Johns Hopkins University and holds a Master’s in Clinical Informatics Management from Stanford University School of Medicine.
Product Management Leader, Maxis AI
Varsha Kishore Product Management Leader·Maxis AI Varsha Kishore is a strategic Product Management Leader at MaxisIT, where she spearheads the conceptualization and end-to-end delivery of flagship Agentic AI products. With over ten years of experience in clinical IT and Pharmaceutical industry, she has evolved from a high-impact Business Analyst into a visionary leader specializing in the integration of AI frameworks within GxP-compliant clinical trials. Varsha is recognized for orchestrating high-performing cross-functional teams to drive innovation and operational excellence.
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