Overcoming Barriers to RBQM Adoption
Presenter: Diane LacroixRecorded Live: Thursday, March 30, 2023
Increasingly complex drug development, rapidly accelerating volume of clinical data, and regulatory requirements, combined with productivity pressures mean that risk-based quality management (RBQM) is an increasingly crucial approach. However, adopting RBQM is not always straightforward, and clinical data management and clinical operations teams often face change management and internal alignment challenges when introducing risk-informed approaches.
This 30-minute webinar, presented by eClinical Solutions’ VP Clinical Data Management, Diane Lacroix, will explore practical steps that organizations can take to overcome common RBQM adoption issues. Drawing on her extensive experience of incorporating innovations to enhance eClinical’s Biometrics Services, Diane will discuss how to take the first steps towards RBQM adoption, share a real-world adoption case study, and highlight outcomes and practical tips for success.
What You Will Learn
- The common barriers to RBQM adoption
- Practical steps towards introducing RBQM approaches
- Key lessons learned from eClinical Solutions’ RBQM journey
- Achievable outcomes
If you’re a clinical data management or clinical operations professional who wants to gain practical, actionable insights to inform RBQM adoption and stay ahead of this rapidly changing landscape, join us on March 30th.
Diane LacroixVice President, Clinical Data Management, eClinical Solutions
Diane Lacroix is a data management professional and leader with over 20 years in the pharmaceutical/CRO industry. As VP, Clinical Data Management at eClinical Solutions, Diane is responsible for leading the data management function including building effective process and implementation strategies to ensure that clients receive maximum value and quality from the elluminate driven data services that Diane’s team delivers. Diane’s career in data management has included numerous leadership roles both at service providers and on the sponsor side. She has worked on all aspects of global trials from study start-up through to database closure and submission leading and managing successful teams and projects to ensure high quality and on-time delivery of clinical data assets. Diane has deep expertise in the oncology and rare disease therapeutic areas and in data management technologies including EDC (Electronic Data Capture) systems and integration and analytics technology platform like elluminate.