Reduce Live Study Risk With AI in eClinical Workflows

Artificial intelligence is rapidly entering the clinical trial ecosystem, and clinical operations and data management leaders are under pressure to understand where it can reduce risk in live studies. This webinar explores how AI is being applied across eClinical workflows to improve data quality, accelerate review and strengthen oversight without disrupting ongoing trials.

As eClinical systems become more connected, trials are generating increasing volumes of data from EDC, eCOA, RTSM, labs, wearables, imaging, safety systems and external vendors. Manual review models are under growing pressure as data volumes rise, timelines compress and sponsors, CROs and sites are asked to do more with the same or fewer resources.

The featured speakers will discuss practical use cases already being applied in live studies, including data review, repetitive check automation, anomaly detection, medical coding, reconciliation, operational forecasting and continuous oversight. The webinar will also examine common implementation risks, such as fragmented source systems, interoperability challenges, validation requirements, documentation gaps and the need for meaningful human oversight in regulated clinical environments.

Attendees will learn how sponsors, CROs and sites can build readiness across clinical data management and clinical operations teams while maintaining data quality, regulatory transparency and study continuity.

Register for this webinar to learn how eClinical workflows can support AI adoption, reduce risk, increase efficiency and strengthen oversight in live studies.

Speakers

Joby John, Vice President, Service Delivery, Sitero

As Vice President of Service Delivery of Sitero’s Mentor eClinical Technology, Dr. John oversees professional and managed services for our eClinical products, as well as our Clinical Data Management and Biostatistics offerings. Dr. John is a Senior Clinical Research leader with over 20 years of global leadership experience. She has worked with a wide array of global pharma companies, CROs and FSPs and has been involved in building up and managing multiple clinical domain teams. She is passionate about clinical data management and its evolution and has presented/chaired sessions in multiple industry forums, including DIA and SCDM. Prior to working at Sitero, Dr. John worked with Clario, Bioclinica and Accenture in leading large global teams delivering clinical services.

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Aman Thukral, Head of Digital Operations & Clinical Systems, Abbvie

Aman Thukral is the head of Digital Operations & Clinical Systems at Abbvie. He has over Nineteen years of experience in clinical development, technology planning & business-technology alignment. He is responsible for Clinical Data Repository, eCOA operations, wearables, and sensors and for piloting new technology initiatives. Before this position, he had worked at various levels at Deloitte, Cognizant & GlaxoSmithKline.

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Charlene Dark, COO of Avania

As Chief Operating Officer of Avania, Charlene Dark leads at the intersection of people, operations, and change. She is known for asking difficult questions, creating clarity in complex situations, and helping teams move beyond established practices when a better path is possible. With extensive experience leading global clinical research operations, Charlene understands that reducing study risk requires more than technology. It requires trusted data, clear accountability, and leaders who empower people to act on what they see. She brings that perspective to the use of AI in eClinical workflows, focusing on how it can help study teams recognize risk sooner and respond more effectively. Charlene is also the author of Mindset Reimagined.

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