CROs are often at the forefront of adopting new technologies to make clinical trials more efficient. Hear how ICON, Lotus Clinical Research, and Bioforum are speeding database builds and automating reporting tasks for data management. They’ll share insights into how to:

  • Build a database from standards and your protocol (not a spec)
  • Replace manual documentation with system-generated reports
  • Provide real-time visibility into the status of data collection and cleaning

Hear their first-hand accounts of adopting an Agile Design methodology with Veeva Vault CDMS and reaping the rewards of a straightforward build and a modern EDC.

Featured Speakers

Harbal Sidhu

Senior Manager, Data Management

Harbal Sidhu is a Senior Manager in Data Management at ICON Plc. Harbal leads ICON’s CDMS delivery for SaaS and homegrown EDC systems. He has over 13 years of EDC programming experience and is the business system owner for Veeva CDMS. Harbal holds a Bachelor’s Degree in Information Science & Engineering. 

Tanya du Plessis

Vice President, Data Strategies and Solutions
Bioforum the Data Masters

As a certified clinical data manager, Tanya holds a M.Med.Sc in Hematology and Cell Biology from University of the Free State, as well as her project management professional certification. She has vast industry experience with over 14 years with IQVIA (legacy Quintiles). As manager of various data management operation teams, Tanya has actively lead strategies for customized data delivery solutions focusing on timely quality data. She has driven numerous innovation teams, and her dedication to optimal customer service/delivery is visible through her long standing relationships.

Jennifer Nezzer

Director of Biometrics
Lotus Clinical Research

Jennifer Nezzer is the Director of Biometrics at Lotus, Clinical Research. Home based in Austin, TX, as the head of the biostatistics and data management departments, she is responsible for the recruitment and management of team members, providing technical leadership on the data management and biostatistical aspects of all development projects as well as serving as lead statistician on multiple programs. Prior to joining Lotus, she was a member of the biostatistics leadership team at Premier Research and supported the biostatistical development of numerous global programs at Premier and PPD for more than 10 years.

Andrea Kreuger

Clinical Data Manager
Lotus Clinical Research

Andrea is a Clinical Data Manager with a demonstrated history of working in the research industry. She is a strong research professional skilled in Clinical Data Management, Market Research, Management, CRO Management, and Business Process Improvement.

Dan Crawford

Senior Director, Vault CDMS Strategy
Veeva Systems

Dan has worked in the pharmaceutical industry for more than 25 years. He has participated in or had oversight for hundreds of clinical trials across various therapeutic areas. Dan is a member of the CDISC-CDASH core team and CDASH CFAST Expanded Leadership Team. In addition, he has performed clinical assessments to assess compliance and provide oversight on adherence to SDTM standards/FDA submissions. Currently Dan is senior director, CDMS strategy where he is responsible for growing CDMS in the CRO space.


Register now for this webinar