Decentralised Clinical Trials

        7 – 9 September 2022, live online training

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        Summary

        Decentralised clinical trials have been on the rise for several years, but the effects of the recent pandemic have accelerated their adoption and further underlined their benefits. Speed to market without compromising quality is the most critical success factor. This 3-day course will outline how DCTs can address under enrollment, high dropout rates and reduce duration, costs, and budget overruns in clinical studies.

        Learning Objectives

        • Learn how to design protocols for DCTs
        • Understand the opportunities & challenges of DCTs
        • Take advantage of electronic tools
        • Deal with patient recruitment challenges
        • Overcome data management & protection requirements

        Key Topics

        • Key definitions concerning DCTs
        • Data management
        • Patient recruitment
        • eTools
        • Site staff/investigator responsibilities
        • Challenges and opportunities for companies

        Who should attend?

        • Quality Assurance, Monitors
        • Clinical Research Associates
        • Clinical Scientists
        • Clinical Trial Managers
        • Regulatory Managers
        • Quality & Compliance Managers
        • Investigators & Site Staff
        • Project Team Members
        • Legal Team Members
        • CROs, Consultants, Insurers

        Our online training experience includes

        • Our client zone – a single source for all training materials as well as pre and post-training communication
        • Live interactive format via the Zoom platform
        • Direct interaction with the trainer
        • Q&As, case studies, polls
        • Revisit recorded sessions for 30 days
        • Training in digital format
        • Digital and LinkedIn certificates

        Trainers

        Dr. Karin Koehler-Hansner
        Clinical Research Consultant & Quality Specialist
        Through more than 17 years of experience with high-ranking, international pharmaceutical and biotechnological companies as well as Contract Research Organizations Karin has acquired proven expertise in the field of clinical research and compliance with high quality standards. As a trained biologist with a PhD in cancer research Karin started her career in clinical research as a Freelance CRA.

        Decentralised Clinical Trials

        Download the full training agenda to reveal complete session details, training takeaways, case studies, daily schedule, special features and full trainer bio.

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        Online Participation
        1 650 € Price incl. VAT: 1 650 €
        Equivalent of approx. 1 777 USD.
        The price calculation in USD is informative and might slightly differ from your bank exchange rate        .

        Price per delegate including:

        Online participation

        Online workbook & materials

        Certificate

        PC, microphone, camera, stable internet connection and the Zoom application.

        Yes, we will make every effort to ensure best possible interaction. You will see the slides, interact with the trainer and fellow participants. Questions and group exercises will be facilitated through the online meeting platform.

        Yes, you can transfer the registration to a colleague at any time.

        Yes, you may transfer your registration to a different event up to one month before the scheduled dates, provided the training fee has been paid in full.

        pharma learning leader

        Lydia Makori

        l.makori@symmetric.events
        +421 222 200 543

        Training Details
        • Start Date
          7. September 2022
          09:00 AM Vienna time
          08:00 AM London time
          03:00 AM New York time
          12:00 AM Los Angeles time
        • End Date
          9. September 2022
        • Email
          l.makori@symmetric.events
        Request in-house