Digital processes such as eConsent are becoming essential for today’s clinical trials. However, there’s more to consider than just asking participants to electronically sign a consent form. Integrating eConsent into trials spans form design, sponsor and institutional review board (IRB approvals), as well as site and participant ease of use.
Register for this webinar to hear representatives from Bioclinica discuss these considerations and demonstrate how Bioclinica eConsent enables an electronic informed consent process from start to finish, including:
- Improved participant understanding by integrating other digital technologies such as videos and voiceovers into the informed consent process
- Reduction of site burden with an intuitive interface
- Incorporating IRB review and approval into the system itself
Speakers
Richard Murg, Global Vice President, Business Development, Bioclinica Software Solutions
Richard Murg is the Global Vice President of Business Development for the Software Solutions Division of Bioclinica. He is responsible for Sales and Marketing and very influential in the operations and development of the products and services. Richard started his career in finance as an analyst at Disney and eventually moved into software sales.
Richard came to Bioclinica in 2006 as the West Coast Account Executive. In 2016, he was named the Vice President of Sales Mid-Markets. By the time he left Bioclinica, he was responsible for more than $100M in sales. Richard was then tapped to be the Chief Revenue Officer at MedNet Solutions in 2017. He increased the company’s sales by 25% and led them to record bookings in 2018.
Richard returned to Bioclinica in 2019 to restore the company he loves. Richard is a West Point graduate, has earned an MBA and is a war veteran.
Message Presenter
Blain Young, Pre-Sales Solutions Consultant, Bioclinica Software Solutions
Blain Young is Bioclinica’s lead Solutions Consultant with over 6 years in eClinical and medical device experience, specializing in operational and data management applications. He is a certified in eConsent, EDC, ePRO/eCOA, RTSM, CTMS, eTMF. Blain acts as trusted advisor for Bioclinica solutions to global sales team and customers. He recently configured the Pre-Sales demonstration environment for the eConsent application.
Message PresenterWho Should Attend?
This webinar is suitable for managers, leads and other relevant job titles in the following departments:
- Medical Directors
- VP, Clinical Operations
- Director, Clinical Operations
- Associate Director, Clinical Operations
- Manager, Clinical Operations
- Clinical Research Associates
- Clinical Study Managers
- Data Analysts
- Data Managers
- Project Managers
- Monitors
What You Will Learn
In this webinar, participants will learn about:
- Improved participant understanding by integrating other digital technologies such as videos and voiceovers into the informed consent process
- Reducing the site burden with an intuitive interface
- Incorporating IRB review and approval into the system itself
Xtalks Partner
Bioclinica
Bioclinica is a global, life-science provider that utilizes science and technology to reduce risk of clinical trials – helping companies to develop new, life-improving therapies more efficiently and safely. The company’s offerings include medical imaging and cardiac safety services; clinical adjudication; randomization and trial supply management and optimization; electronic and eSource data capture; site and patient payments and budget forecasting; pharmacovigilance, and trial management.
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