Nancy Meyerson-Hess

Chief Compliance and Regulatory Officer - eMQT

Nancy Meyerson-Hess has over 30 years of experience in leading global clinical research teams in pharmaceutical and contract research organizations.


She has focused on providing best practices for success in global clinical research, including emerging regions, in areas such as Good Clinical Practice and Inspection Readiness. In addition, she has extensive experience in patient-centered activities and solutions.


Nancy provides consultant support to pharma and biotech, as well as organizations specialized in emerging regions and patient engagement for clinical research and clinical trials, with a focus on quality and process improvement.


Nancy is located in Munich, Germany.

Nancy Meyerson-Hess


  • Wednesday - September 21, 2022 - 09:40

    Chairperson’s opening remarks

  • Wednesday - September 21, 2022 - 14:15

    Panel discussion: Effective patient recruitment and retention in clinical trials to boost trial success

    • What will persuade and impact the patient?
    • Is there anything pharma can provide for a trial member that will increase the value of participation?
    • The aim of patient-driven clinical trials is to diminish the burden of participation by making the participant journey as convenient and pleasant as possible
    • Utilize fitting procedures and techniques to limit dropouts without, in any capacity, constraining a patient to remain in the study
    • Utilize wider use of the innovative statistical and Machine Learning techniques to provide more accurate data-driven forecasting and centralized monitoring of patient recruitment

  • Wednesday - September 21, 2022 - 17:55

    Panel discussion: The patient's perspective: why their voice is so important in clinical research

  • Wednesday - September 21, 2022 - 18:25

    Chairperson’s closing remarks

  • Thursday - September 22, 2022 - 09:50

    Chairperson’s opening remarks

  • Thursday - September 22, 2022 - 14:45

    Panel Discussion - A collaborative clinical ecosystem: How to effectively manage partnerships with all Stakeholders including Patients, Sites, CROs, Sponsors and Regulators.

  • Thursday - September 22, 2022 - 16:55

    Panel Discussion: The Future of Clinical Trials - The Role of Advanced Analytics and Artificial Intelligence

  • Thursday - September 22, 2022 - 17:50

    Chairperson’s closing remarks


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