Improving clinical trial efficiency using Real-World Data
Reactions of participants:
“Thank you very much for your training, I learnt a lot and I realized I need to learn even more ! It was very informative and well done.”
“Thanks for such a well run and interesting workshop. I learnt loads – especially about synthetic control arms. It was also great to see everyone participating.”
““The breakout sessions are good for networking, like speed dating”
About the trainer(s):
Berber Snoeijer started in clinical research in 1997 as a biometrician and has since then worked with clinical data in different functions. In 2001, she founded a CRO, Biometric Support, focussing on data management, data analysis, and reporting of clinical trials. Ten years later, in 2011, she started working as an R&D manager dedicated to investigate and utilise the potential of real-world data from electronic health records. This resulted in many different solutions including a full reporting system to give feedback information to clinical research professionals. In order to enhance the efficiency of processes and data use, she applied her skills of technical (software and database) engineering, process engineering and improved efficient utilisation of and interactions between people based on management drives. Nowadays, she uses her skills and knowledge to assess, design, and improve business solutions and processes on small and large scales.
Berber is chair of the PHUSE real-world evidence project, real-world evidence stream chair of the PHUSE EU CONNECT and member of the EUCROF real-world evidence workgroup.