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Evaluating Global eConsent Use Cases – Supporting Patient Engagement and Comprehension


Sep 17, 2020 07:24 AM

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Christian Knaus
Senior Director, Client Development @snapIoT
Christian has worked globally in clinical trials since 2006. At what was then known as VIASYS Clinical Research (now ERT) he accrued his first acumen in the Respiratory field as a Project Manager producing Spirometry Solutions as well as ePRO devices with PEF-Meters for clinician as well as patient home monitoring and adding Cardiac Safety and all things eCOA to his experience portfolio over the years. Since 2016, Christian has spearheaded the path toward paperless clinical trials including eCOA solutions, BYOD solutions and wearables. In his role at ICON, he was at the forefront of the SaaS movement for clinical app development where he was instrumental in building an industry leading eCOA team of Project Managers that spans the US, UK and Germany.
Karla MacKenzie
Head of Site Management and Virtual Clinical Trials Oceania @Studies&Me / LEO Pharma
Karla MacKenzie is an international Clinical Trials innovator, speaker & consultant on Digital Strategy and Innovations in Clinical Trials at Studies&Me and Leo Pharma. Karla is passionate about empowering patients and Pharma companies to deliver better medicines for the benefit of all patients. After a successful international career at Sanofi, GSK and LEO pharma, Karla combines her skills to adapt to the new exigencies of digitally enhanced clinical trials. Above all, Karla works to catalyse a change in mindset and dial up transformation across organisations. Karla received her B Pharm at Otago University and her MSC (Hons) at Massey University in New Zealand before embarking on a Clinical trials career. She has solid people and stakeholder leadership skills demonstrated in 20 years directing programmes, leading international cross functional teams, implementation of over 50 complex projects in over 54 countries.
Melanie Flores, CIP, CCRP
President @IntegReview IRB
Melanie is the President of IntegReview IRB. She is responsible for the implementation of the organization’s vision, mission, and overall direction by upholding a respectful and ethical company culture and ensuring production efficiency, quality, and service. She implements company strategic planning in an effort to ensure the protection of the rights and welfare of human subjects involved in research. Melanie provides continuous training, education and guidance for IRB staff, IRB members and clients to ensure compliance with Federal Regulations, ICH Guidelines, IntegReview IRB SOPs and AAHRPP standards. She has worked in the IRB industry since 1999.