On the 21st of July 2020 CROS NT conducted a webinar focused on clinical trial data oversight.
During the webinar titled “Clinical Trial Data Oversight: Why and How?”, we reviewed oversight as it relates to data collection and reporting, analysed options for oversight including an assessment of different approaches, discussed the benefits of a centralized approach to data and presented case studies.
Webinar learning outcomes:
• Understanding of the importance of oversight for clinical trial data
• Understanding oversight options and choosing the right approach
The webinar was presented by:
– Amanda Cross, Country Manager US and Executive Director of Service Strategies of CROS NT
Amanda joined CROS NT in 2018 and oversees all operations and business strategy for the U.S. branch of CROS NT. She also manages the strategy for the Biometrics Optimization Solution helping clients to design and implement oversight strategies and a centralized data approach. She is a biostatistician by background and training having started her career in 1995. Amanda has worked in biostatistics and biometrics operations in both the pharmaceutical and CRO sectors with experience in multinationals as well as small to mid-size companies. She also holds a degree in Statistics from Virginia Tech.
– Antonella Bacchieri, Senior Consultant Statistician of CROS NT
Antonella has worked in the pharmaceutical industry and in Contract Research Organizations for almost 30 years, with extensive experience in biostatistics and data management. As Senior Consultant Statistician in CROS NT, Antonella is responsible for providing statistical consultancy services for multiple clinical studies alongside designing and optimising.