Audio Conference

Optimizing CRA Deployment in Global Clinical Trials Marie Snell Director, Clinical Project Management Covance Recording US$199

Purchase a recording of this Audio Conference

This audio conference will provide insight into how to drive ROI by optimizing CRA deployment and data management staff planning. Specifically, the presentation will detail the critical patient data that should be captured in your IVR system in order to maximize the efficiency and organization of CRA site visits. This data can then be linked with your clinical trial management system to project the data workload accumulated at investigator sites. The speaker will provide practical examples of how this information has been used to optimize deployment of CRAs to investigator sites and to drive efficiencies in those site visits. Furthermore, the presentation will examine how the IVRS data stream can also be used to determine the amount of data management staff that will be required in the trial. More effective utilization of an IVRS data stream can enhance visibility into trial performance and drive cost-saving efficiencies.

This audio conference will address:

• Critical patient data parameters that should be captured in the IVR system
• The criticality of effective linkage between IVR and clinical trial management systems in terms of realizing cost-saving benefits
• How IVR data can be used to optimize CRA deployment schedules and maximize visit efficiencies - with examples
• The ROI benefits of effective management of CRA visits and optimization of data management staff requirements

Speaker biography:

Marie Snell has a strong background in science and research, having spent 10 years in public health, another five in an academic research setting, and 11 years in the CRO industry as a CRA, project manager and project director. In her current role with Covance, Marie oversees clinical project teams and also serves as process owner for Six Sigma projects. Prior to joining Covance in 1996, she spent several years at Vanderbilt University, working on several NIH and NASA-funded studies and assisting with development of protocols and procedures. Since joining Covance, she has developed a broad base of indication experience, with particular strengths in sexual dysfunction, psoriasis, pulmonary disease, and vaccine studies relating to flu and HPV16-related cancer.

Marie received her BS in Environmental Science from Troy State University in Troy, Alabama, with additional post-graduate studies at Mercer University in Macon, Georgia, and Tennessee State University and Nashville State Technical University in Nashville Tennessee.

Who Should Attend?

• Clinical Project Managers
• Data Management
• Clinical Trials Operations
• Outsourcing Directors and VPs
• Senior Management
• Clinical Directors and VPs
• Global Project Directors
• Senior Clinical Managers
• Senior Operational Managers
  

Purchase Options:

• Purchase a recording of this event US$199