eClinical & Clinical Data Management Innovation Virtual Conference
Virtual Event
2nd June 2021
eClinical & Clinical Data Management Innovation Virtual Conference
We are pleased to announce the launch of a brand new event: The eClinical & Clinical Data Management Innovation Conference will take place on 2nd June 2021!
This event has been exclusively designed for the cutting-edge data & analytics leader, focused on aligning data strategy with digital transformation, leveraging data analytics to increase business value and use data to promote growth.
The 2021 programme will feature a range of speakers from the likes of GlaxoSmithKline, AstraZeneca, Pfizer, Shire any many more, who through a variety of interactive session formats will offer insight on promoting successful eClinical and clinical data management.
We look forward to seeing you (virtually!) there
A FANTASTIC NETWORK OF YOUR PEERS AND COLLEAGUES RIGHT AT A TAP OR CLICK OF A BUTTON
Simply register, login on the day and get ready to connect and learn. With the right network at your fingertips, catching up with your peers has never been so easy – even from a distance.
TESTIMONIALS
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‘That was a superb day, it feels like we’ve been at a real, in person, conference!’ Worldwide Clinical Trials
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‘A great event, I met more people than I do at an in-person event and I’ve got loads of follow ups’ Conversis
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‘The whole setting is actually very well accomplished! Thanks again for the invitation!’ Apogenix AG

Ken Getz
Director, Research Professor,Tufts Center for the Study of Drug Development
Biography: Ken is the Director of Sponsored Research and Associate Professor at the Tufts Center for the Study of Drug Development, and Chairman of the Center for Information and Study on Clinical Research Participation, a non-profit organization that he founded to raise public and patient awareness of the clinical research enterprise. He is founder and owner of CenterWatch, and an owner and board member of the Metrics Champion Consortium. A well-known speaker at symposia, universities, and corporations, Ken has published extensively in peer-reviewed journals, books and in the trade press. He has been an active DIA member for 25 years and has held board appointments in the private and public sectors. Ken earned his MBA from Northwestern University.
Session Details: Keynote: Monitoring e-Clinical Data To Identify New Growth Points 02-06-2021, 8:00 am View In Agenda

Terry Katz
Sr Director, Biostatistics and Data Management Planning and Functional Excellence,Daiichi Sankyo

Pieter Voermans
Head Clinical Data Management,SOBI
Biography: Experienced (20+ years) Clinical Development Leader specialised in Data Management with broad international Drug Development expertise and wide industry knowledge (small Biotech to large Pharma) with a passion for leading cross-functional teams to successful delivery
Session Details: Techniques To Best Manage Your Data More Effi-ciently Throughout Your Study Cycle 02-06-2021, 9:00 am View In Agenda

Krishna Mankala
Executive Director,SK Life Science
Biography:
Session Details: Considerations Needed When Digitalising Your Clinical Trial 02-06-2021, 9:00 am View In Agenda

Jacqueline Gough
Director Centralized Monitoring and Data Surveillance,Astellas Pharmaceuticals
Biography:
Session Details: Implementing Centralised Monitoring Processes To Support Current Trials 02-06-2021, 11:00 am View In Agenda

Craig Lipset
Co-Chair,Decentralised Trials and Research Alliance
Biography:
Session Details: Looking To The Future: Assessing Innovative Trends That Will Help Shape e-Clinical Landscape 02-06-2021, 11:00 am View In Agenda

Aman Thukral
Head of Digital Operations and eCOA,AbbVie
Biography:
Session Details: Fireside Chat: Analysing Digital Devices In Harnessing Real World Data 02-06-2021, 3:20 pm View In Agenda

Patrick Zbyszewski
Director, Data Management and Programming,Endo Pharmaceuticals
Biography:
Session Details: Q&A: Considerations When Working With Multiple Sites and Collecting Study Data 02-06-2021, 2:20 pm View In Agenda

Swapna Bapat
IT Manager,Janssen
Biography:
Session Details: Panel: Decentralising Your Clinical Trials But Achieving Optimum Results 02-06-2021, 2:50 pm View In Agenda

Frances Rubenstein
Director, Database Management,Nevro Corp
Biography: Dr Frances Rubenstein has worked in clinical data management for 20 years in both medical device and pharmaceutical companies. She has extensive experience in leading data management activities for multiregional clinical trials in all phases and several therapeutic areas. Frances has an undergraduate degree in Physiology and a PhD in medical science from the University of Sydney. Frances has been working at Nevro Corp, a medical device company for the past 9 years as Director, Database Management. In her role at Nevro, Frances is responsible for selecting and managing vendors and technology to deliver quality clinical trial data to support decisions that bring new treatment to patients.
Session Details: Outlining the necessary procedure to prepare for FDA submission for MedDevice 02-06-2021, 3:20 pm View In Agenda

Rosanne Petros
Associate Director, Clinical Research Manager,Merck

Vladimir Anisimov
Data Scientist,Amgen
Biography:
Session Details: Innovative AI technologies for data-driven forecasting & monitoring patient recruitment & trial operational design 02-06-2021, 12:30 pm View In Agenda

Vanja Vlajnic
Senior Manager, Statistics and Data Insights,Bayer
Biography: Vanja Vlajnic is a Bayer Science Fellow and Sr. Manager within the Statistics and Data Insights function, supporting the late-stage cardiovascular franchise at Bayer. He is the co-lead of the Biostatistics Innovation Center Data Mining group and is highly involved in developing strategies for the analysis of high-dimensional data in the clinical space. Vanja has a Master’s of Applied Statistics from Penn State University, a Master’s of Experimental Psychology with a focus in Behavioral Neuroscience from Seton Hall University, and is a Ph.D. candidate in Systems Engineering with a focus on Biomedical Engineering from Colorado State University. He has published in the areas of machine learning applications to clinical data, causal learning and causal inference, clinical assessment tools in schizophrenia, and visual perception. He is a member of the IDSWG AI subteam, Phi Beta Kappa, the American Statistical Association, and the Vision Sciences Society.
Session Details: Expanding Upon The Utility and Versatility of Decentralized Clinical Trials Through the Use of Digital Endpoints 02-06-2021, 12:00 pm View In Agenda

Amy Cramer
Director of eSource,Pfizer
Biography:
Session Details: Panel: Connecting Clinical Research and Healthcare: The Vulcan HL7 Accelerator Opportunity 02-06-2021, 12:00 pm View In Agenda

Prasun J Mishra
Founder CEO,Agility Pharmaceuticals
Biography: Dr. Mishra (Ex-Genentech, Ex-NCI, Ex-NIH) is the Founder and CEO of Agility Pharmaceuticals. He is a serial entrepreneur who founded his first company after graduating high school, and second company during his PhD. Since then, he has accumulated a wealth of experienced by building, investing and advising numerous other companies. He is an investor/ co-founder/ board member of a few US based corporations focused on accelerating drug discovery & development, blockchain & digital health. Dr. Mishra is also founding president & CEO of American Association for Precision Medicine (AAPM) and is leading research efforts focused on preventing & curing chronic diseases; not only treating the sick but also providing knowledge/tools to individuals to live longer, healthier lives. Widely recognized as a thought leader in the field of Technology and Healthcare, Dr. Mishra has keynoted, chaired, curated and organized numerous successful international conferences. Prior to Agility Pharma, Dr. Mishra served as a scientist and Principal Investigator at Genentech, Roche. Moreover, his passion for drug development and precision medicine has led to identification of new drug targets, biomarkers, companion diagnostics and several drugs/ combinations in the clinic. His research work has been recognized globally by over 40 prestigious awards and honors. Due to his unique perspective & selfless service, he is highly respected & sought-after mentor to many. The companies that he has advised have raised multimillion dollars. Notably, he serves as a mentor and advisor to startup accelerators such as IndieBio, Health2.0’s Project Zygote and CLSI FAST program, to help grow California’s life sciences innovation ecosystem.
Session Details: Convergence of Big Data and Artificial Intelligence in Augmenting Drug Discovery, Development and Supply Chain Management 02-06-2021, 3:50 pm View In Agenda

Gian Prakash
Associate Director, R&D Information Research,AbbVie
Biography:
Session Details: Measuring Clinical Data De-Identification For Enabling Secondary Research and Drug Discovery 02-06-2021, 3:50 pm View In Agenda

Sam Hume
Head of Data Exchange Technologies,CDISC
Biography:
Session Details: CDISC To Drive Standards-Based Automation as It Supports e-Clinical and Data Management 02-06-2021, 8:00 am View In Agenda

Revati Tatake
PhD, Global Director of Databases and Analytics,GlobalData
Biography: Revati Tatake currently serves as a Global Director of Databases and Analytics at GlobalData, where her primary responsibilities are to lead the development and continuous enhancement of integrated databases and analytical tools for providing competitive and business intelligence for pharmaceutical and biotechnology sectors Revati has more than 20 years’ experience, both in academic research and the healthcare industry, during which time she focused on basic and clinical research, drug discovery and competitive intelligence projects across many therapeutic areas. After academic career at Tata Cancer Research Institute and the University of Connecticut Health Center, she began her healthcare industry career at Boehringer Ingelheim Pharmaceuticals, where she led drug discovery projects involving small molecules, gene therapy and cell therapy for cardiovascular diseases, Rheumatoid arthritis and Diabetes. In addition to leading drug discovery projects, Revati co-chaired novel target identification group, scouted novel technologies for enhancing drug discovery efforts, established collaborations with experts in academic institutions to complement internal projects and evaluated in-licensing opportunities for their scientific and technical merit. She is a co-inventor on several issued US patents and applications related to the projects on cell and gene therapies. Before joining GlobalData, Revati worked at Citeline, where she was involved in competitive intelligence and analytics of clinical trials and pharmaceutical products. Revati holds a PhD in Tumor Immunology from Tata Cancer Research Institute. She was a post-doctoral fellow at the University of Connecticut Health Center.
Session Details: An Analytical Overview on Decentralized trials and Where The Industry Is At 02-06-2021, 4:20 pm View In Agenda

Max Horneck
Head of Clinical Data Management and eClinical Systems,Medac GmbH
Biography: Max Horneck has been the programmer and developer of one of the first EDC and IRT systems in the young internet-era in the 90s. For more than 25 years he worked in clinical IT and data management. He has a PhD in linguistics, philosophy and computer science. Currently he holds a position as head of clinical data management and eClinical systems at medac GmbH a midsize pharmaceutical manufacturer. With more than 20 years of CRO background, 10 years business consultancy and 5 years in pharmaceutical industry he combines the perspective of a CRO with that of a sponsor organization.
Session Details: Roundtable 02-06-2021, 10:20 am Roundtable 02-06-2021, 10:20 am Sponsor Oversight in Managing Real Time Data 02-06-2021, 12:30 pm View In Agenda
Sponsors




IQVIA Technologies
Sponsorship opportunities
To enquire about sponsorship opportunities for the conference, please contact:
Conor Taylor
Portfolio Lead – Oncology and Clinical Data
Zoom: +44 207 947 2711
E: conor.taylor@arena-international.com
Speaker Opportunities
The 2021 programme is written in collaboration with industry, if you have a case study, idea or just a comment, please contact:
James Reidy
Programme Director
Zoom Direct: +44 (0) 20 7661 0879
james.reidy@arena-international.com