Clinical Operations teams face mounting pressure to manage growing data complexity, ensure regulatory compliance, and mitigate risks—all while meeting tight timelines. Traditional methods often lead to inefficiencies, fragmented oversight, and delayed insights.
In this exclusive webinar, discover how DTect AI, an innovative AI-powered platform, helps life sciences organizations optimize clinical trial data quality management. DTect AI transforms Integrated Data Review (IDR) and Risk-Based Quality Management (RBQM) processes ensuring and unmatched data integrity and significantly reducing data management cycle times.
Key Learnings:
What Makes DTect AI Stand Out?
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Data Analytics and Engineering Leader
Jayasree has 15.6 years of experience in providing analytical solutions using business intelligence and analytical tools. Primarily focuses on understanding key analytical challenges in pharmaceutical environment and working closely with key stakeholders across clinical operations. Expertized in building advanced analytical solutions that establish insights into data, providing signals, patterns, trends, and works across different functions to break down barriers between silos while providing a data-driven integrated & holistic view to end users.
Sr. Principal Clinical Data Scientist & Tech-Lead Solution Owner
Matt Callahan, a seasoned Sr. Principal Clinical Data Scientist with over 15 years of experience, specializes in advancing pharmacovigilance, patient safety, and risk-based monitoring (RBM) through innovative clinical analytics and Data Science-as-a-Service (DSaaS) tools. At MaxisIT, he supports neurodegenerative disease, oncology, and immuno-oncology programs across Phase I-III trials, driving solutions that enhance data quality, streamline workflows, and empower data-driven decisions. With expertise in computational biology, biomedical science, biostatistics, and project management, Matt is dedicated to delivering impactful informatics solutions that optimize clinical operations.
MaxisIT helps pharmaceutical and biopharmaceutical companies of all sizes plan and execute effective clinical trials. Our source-agnostic integrated clinical data analytics platform unifies data across clinical systems and CROs to enable real-time monitoring and on-time insights.