Webinar: The Evolution of Data Management

Watch our webinar and get ready for the future of clinical research


Clinical research today would be unrecognizable to yesterday’s data managers. Watch our webinar, The Evolution of Data Management, for insight into where we came from, where we’re headed, and how best to position your organization for success. Gina Budman, a clinical data management consultant, and Laurin Willetts, Customer Success Manager at Medrio, dive deep into a variety of topics to facilitate an understanding of where we stand at this pivotal time for our industry.

Key takeaways:
  • How data management roles have changed with the advent of eClinical technology
  • Why successful organizations are adopting cloud-based eClinical systems
  • How to succeed amid increasing globalization and technological advancement
Presented by
Gina Budman
CEO and Founder, Leading Edge CDM

Gina Budman is a founder of LeCDMS (Leading Edge CDM Solutions), Clinical Data Advocates organization. As LeCDMS CEO and Principal Consultant, Gina ensures her teams – CDMs, Biostatisticians, Programmers and Validators – become trusted partners to their clients and deliver data of highest quality and compliance.

Gina has over 20 years of Clinical Data Management experience, and prior to that, 14 years of Project Management and Programming/technology. She worked as a Clinical Database designer, Manager of CDM, Director of CDM, and a data consultant for various industry leaders such as Boston Scientific, Abbott Vascular, and multiple CROs and Sponsors. Gina has created the first EDC course at UCSC Extension, and taught Data Management at various institutions.

Laurin Willetts
Customer Success Manager, Medrio

Laurin Willetts has over fifteen years of experience in clinical trials, program management, and research and development, and has worked in lab and business settings. She been instrumental in managing several clinical trials resulting with FDA clearance, particularly at diagnostics sponsor companies.  Her experience includes building clinical trial programs from the ground up, including processes and infrastructure, site feasibility/selection, contracts/budgets, database build, study start-up, patient enrollment, and metrics.

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