SOCRA Digital Health & Clinical Research Workshop- LIVE
Includes a Live In-Person Event on 09/23/2026 at 10:00 AM (EDT)
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Register
- Member - $295
- Non-member - $370
Goal: To equip clinical research professionals with the knowledge and practical decision-making skills to responsibly integrate digital health technologies and AI throughout the clinical trial lifecycle while ensuring participant protection, regulatory compliance, operational excellence, and scientific integrity.
Member Rate: $295.00
Non-Member Rate: $370.00
Please book your room here: SOCRA 2026 Annual Conference - Start your reservation
Objective: To provide participants with a practical framework for evaluating, implementing, and governing digital health technologies and AI across the clinical trial lifecycle, enabling them to make informed decisions that enhance research quality, operational efficiency, participant experience, and regulatory compliance. Please contact us with any questions or concerns at [email protected].
Learning Objectives: Upon completion of the workshop, the attendee should be able to:
- Evaluate opportunities to integrate digital health technologies (DHTs), artificial intelligence (AI), digital biomarkers, and real-world evidence across the clinical trial lifecycle to improve research quality, operational efficiency, and participant experience.
- Develop practical strategies for designing and operationalizing decentralized and hybrid clinical trials using digital informed consent, remote participant monitoring, and participant-centered technologies.
- Apply the SMART Framework to evaluate, implement, and govern digital innovation throughout the clinical trial lifecycle while balancing operational efficiency, participant protection, regulatory compliance, and scientific integrity.
- Apply regulatory, ethical, equity, and governance principles to evaluate digital health and AI solutions, including regulatory compliance, bias mitigation, participant protection, human oversight, and responsible implementation.
- Develop practical approaches to digital data management and governance that support data quality, privacy, cybersecurity, interoperability, and research integrity throughout the clinical trial lifecycle.
Please contact us with any questions or concerns at [email protected].
Scott Dixon (Moderator)
Chief Commercial Officer
Curebase
Scott Dixon brings deep experience in life sciences and healthcare technology, having built and scaled high-performing teams around the adoption of digital health technology in clinical research. Throughout his career, he has partnered closely with clinical research teams to bring innovative, software-driven solutions to studies, always balancing operational efficiency with the practical realities of regulatory compliance, data quality, and participant protection. Scott is now Chief Commercial Officer at Curebase, where he leads commercial strategy as the company scales its next-generation eClinical platform, helping study teams across sites, sponsors, and CROs integrate digital tools and AI into clinical trial operations.
Margret (Margo) Kamel, PhD, CCRC (Moderator)
Director of Research Projects in the Division of Pediatric Nephrology
Emory University School of Medicine
Margret (Margo) Kamel, PhD, CCRC, is Director of Research Projects in the Division of Pediatric Nephrology at Emory University School of Medicine, where she oversees the operational, regulatory, financial, and quality aspects of multicenter clinical research at Emory University. With nearly two decades of clinical research experience, she has worked across NIH-funded, industry-sponsored, and investigator-initiated studies.
Dr. Kamel earned her PhD in Health Promotion and Behavior with a concentration in Health Communication and is a Certified Clinical Research Coordinator. Her professional interests include digital tools in clinical research, eConsent, participant engagement, health literacy, research operations, and site–sponsor collaboration. As a facilitator for the SOCRA Digital Health & Clinical Research Workshop, she brings a practical site perspective to integrating digital tools and AI into clinical trial workflows while maintaining human oversight, regulatory accountability, research integrity, and a participant-centered approach.
Teri L. Crumb (Moderator)
Clinical Research Nurse
Teri L. Crumb, MSN, RN, CCRC has more than 25 years of experience as a clinical research nurse. She has presented at national conferences, including MAGI, ACRP, and SOCRA. Teri earned her Bachelor of Science in Nursing (BSN) from Grand Valley State University and her Master of Science in Nursing (MSN) in Clinical Trials Research from Drexel University. She obtained her Certified Clinical Research Coordinator (CCRC) credential through the Association of Clinical Research Professionals (ACRP) in 2005. Teri has been a leader within the Pediatric Nephrology Research Consortium (PNRC), helping develop the TEN (Training, Education, and Networking) Program and serving as Co-Chair of the Coordinator Working Group from 2020 to 2023. Her professional interests include the training, education, and professional development of clinical research staff, promoting careers in clinical research, and strengthening workforce recruitment. In 2022, she founded her own consulting LLC, providing clinical research expertise and support to organizations and research teams.
Muhammad Waseem (Moderator)
Professor of Emergency Medicine and Pediatrics
Weill Cornell Medicine
Dr. Waseem is a Professor of Emergency Medicine and Pediatrics at Weill Cornell Medicine in New York and an accomplished academic physician, clinical investigator, and leader in emergency medicine and pediatric emergency care. He completed his residency in Pediatrics and a fellowship in Pediatric Emergency Medicine, followed by a master’s degree in Clinical Investigation, Epidemiology, and Health Services Research from Cornell University.
For many years, Dr. Waseem has provided institutional and academic leadership as Research Director in the Department of Emergency Medicine and as Vice Chair of the Institutional Review Board (IRB) at Lincoln Medical Center in the Bronx, New York. In these roles, he has advanced clinical research, strengthened research oversight, promoted ethical and responsible conduct of research, and fostered a culture of scholarly inquiry within a high-volume, academically affiliated urban health system.
His expertise spans clinical investigation, research methodology, research ethics, regulatory oversight, and translating research into clinical practice. His commitment to advancing high-quality clinical research is further evidenced by his credentials as a Certified Principal Investigator (CPI) from the Association of Clinical Research Professionals (ACRP) and a Certified Clinical Research Professional (CCRP) from the Society of Clinical Research Associates (SOCRA). Through his roles as a physician, educator, investigator, and research leader, Dr. Waseem has shown a sustained commitment to advancing academic medicine, improving patient care, and developing the next generation of clinicians and clinical investigators
