Enhancing Cardiometabolic Trials with Configurable eCOA and Digital Health Technologies

Biotech, Clinical Trials, Digital Health, Drug Discovery & Development, Pharma,
  • Friday, November 21, 2025 | 11am EST (NA) / 4pm GMT (UK) / 5pm CET (EU-Central)
  • 60 min

In today’s rapidly evolving clinical research landscape, sponsors and CROs seek technology-enabled solutions to simplify study execution, enhance data quality and oversight and encourage patient engagement.

This webinar demonstrates how Clinical ink combines configurable eCOA software and integrated digital health technologies (DHTs), enabling faster study development and robust real-world data collection.

Clinical ink’s solutions offer a unified experience across multiple DHTs, reducing patient burden and ensuring high-quality data collection.

Attendees will learn how Clinical ink’s eCOA platform integrates with leading DHTs, such as continuous glucose monitors (CGMs), blood glucose meters (BGMs), smart weight and body composition scales and wearable physiological data capture devices, to streamline physiological data collection alongside patient-reported outcomes.

By minimizing technical barriers, Clinical ink empowers study teams to deploy technology-enhanced protocols efficiently. Clinical ink’s platform supports near-real-time data flow, providing a comprehensive view of the patient journey.

The featured speakers will share real-world examples of how integrated DHTs have improved data capture, protocol adherence and reduced site and patient burden. The webinar will also cover regulatory considerations for risk assessment and data validation strategies to ensure reliable and compliant sensor-derived data within eCOA workflows.

Register for this webinar to learn how to enhance cardiometabolic trials using configurable eCOA and digital health technologies.

Speakers

Dr. Nicholas Alp, Clinical ink

Nicholas Alp, MD, PhD, FACC, Chief Medical Officer, Clinical ink

Nicholas has more than 30 years of clinical research experience as an academic cardiologist, clinical trialist and commercial drug development expert. Before joining Clinical ink, he was the Senior Vice President and Head of Cardiometabolic Research at Medpace, a global clinical research organization. Previously, Nicholas was Vice President and Global Head of Cardiovascular Drug Development at ICON. He also simultaneously held appointments as a Consultant Interventional Cardiologist at the John Radcliffe Hospital, Oxford and a Senior Academic Appointment in Cardiovascular Medicine at Oxford University.

Nicholas trained in medicine at London University and Oxford University, completed a PhD in Immunology at Cambridge University and earned a postdoctoral Doctor of Medicine (DM) degree in Cardiology at Oxford University. He has also contributed to more than 70 peer-reviewed publications and books.

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Steve Polyak, PhD, Clinical Ink

Steve Polyak, PhD, SVP, Head of Global Product Innovation, Clinical ink

Steve Polyak is the Senior Vice President, Global Head of Product Innovation at Clinical ink, where he leads innovation, architecture and product design for new clinical trial capabilities. His organizational scope includes an innovation lab staffed with engineers, designers and scientists working on connected device integrations, wearables, sensors and digital biomarkers for therapeutic areas including diabetes, weight management, movement disorders such as Parkinson’s disease and ALS. Steve received a PhD in Artificial Intelligence from Edinburgh University in Scotland and a Master’s degree in Computer Science in Chicago. Steve has many years of experience building solutions for large-scale assessments in both health and education markets. Previous work includes innovation at the college entrance exam company ACT, state assessments with Pearson Education, bringing the Encyclopaedia Britannica online and software consulting at Accenture and Computer Sciences Corporation.

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Bill Barrasso, Clinical ink

Bill Barrasso, MBA, Chief Compliance Officer, Clinical ink

Bill Barrasso has years of operational and compliance experience with multiple eCOA service providers. Prior to joining Clinical ink, Bill established the eCOA Services team at Parexel and led eCOA services organizations at both ERT and PHT Corporation. He also held the position of Director of Operations at Concordant Rater Systems (rater monitoring and eCOA data collection in CNS studies), which was acquired by United BioSource Corporation and spun off into Bracket (now Signant Health). Bill earned his MBA at Northeastern University in Boston. He is currently on hiatus from a PhD program for Personal Healthcare Informatics, also at Northeastern University.

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Bill is actively involved in regulatory and clinical issues, process quality, SaMD, data privacy and direct contact with key clients. Bill has developed effective study management processes to improve delivery quality and connect operational study activities to corresponding regulatory, clinical and corporate business functions. Throughout his career, Bill has gained deep experience and knowledge of clinical and regulatory guidance required for successful trial execution.

Bill’s areas of expertise include:

  • Regulatory guidance and Data Privacy (GDPR, Privacy Shield, etc.)
  • Good Clinical Practice (GCP)
  • Clinical Data Management
  • Software as a Medical Device (SaMD)
  • ISO 9001, ISO 13484, ISO 14971
  • eCOA/ePRO data collection technologies
  • CRO operations; licensing and translation services

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Jennifer Guild, Clinical ink

Jennifer Guild, MBA, PMP, Vice President of Strategic Partnerships and Cardiometabolic Operations, Clinical ink

Jennifer Guild is Vice President of Strategic Partnerships and Cardiometabolic Operations at Clinical ink. With more than 15 years of experience in eClinical technologies and drug development, she has built a career at the intersection of clinical operations, digital health and technology-driven transformation.

Jennifer has led global teams across IRT, eCOA and decentralized trial solutions, with expertise spanning risk management, regulatory readiness and operational delivery. Her background includes senior leadership roles at leading health technology organizations, where she oversaw large-scale programs and partnerships supporting some of the world’s leading biopharmaceutical companies. Known for her ability to align stakeholders and guide complex digital health initiatives, Jennifer is passionate about helping sponsors and CROs harness eCOA and digital health technologies (DHT) to improve patient outcomes and operational efficiency in clinical research.

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Jennifer Guild, Clinical ink

(Moderator) Jessica Ryter, MBA, Sr. Director, Product Strategy, Clinical ink

Jessica Ryter serves as the Senior Director of Product Strategy at Clinical ink. With over 13 years of experience in product management and product strategy for clinical software (both clinician and patient-facing), Jessica is a champion for user experience. She is dedicated to translating patient and site feedback into meaningful product enhancements, ensuring that solutions are continually refined to meet the needs of both customers and users. In her role, Jessica oversees Clinical ink’s site and patient experience programs and partners with clients to ensure strategic alignment as the industry evolves. Jessica holds an MBA from Northeastern University in Boston.

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Who Should Attend?

This webinar will appeal to:

  • Sponsors and CRO Executives
  • Clinical Operations Leads
  • Digital Health and Innovation Teams
  • Clinical Data Managers and Biostatisticians
  • Regulatory and Quality Assurance Professionals

What You Will Learn

Attendees will gain insights into:

  • How Clinical ink’s configurable eCOA platform accelerates study builds and enables robust trial design
  • Supported DHT devices, including CGMs, BGMs, smart scales and wearable monitors used in a single trial
  • Benefits of integrating DHTs into eCOA workflows for patients, sites and sponsors
  • Case examples illustrating operational efficiencies and data quality improvements
  • Practical considerations for validation, compliance and data integration

Xtalks Partner

Clinical ink

Clinical ink is a global life science company bringing data, technology, and patient-centric research together. Our deep therapeutic-area expertise, coupled with Direct Data Capture, eCOA, behavioral and dropout prediction, eConsent, telehealth, and digital biomarkers advancements (including use of Continuous Glucose Monitoring for detection of hypoglycemia), support the next generation of clinical trials and ultimately the clinical management of patients.

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