Successful implementation of RBQM is a challenge many in our industry are facing. To understand what it is, how it impacts the management of your clinical trial, and some common misconceptions, this webinar will address:

  • What is E6R2
  • Rho as a case study
    • Designing an implementation strategy
    • Understanding and incorporating E6R2 solutions
  • Lessons learned from Rho’s implementation of RBQM

Featured Speakers

Marina Acosta Enslen

Associate Director, Clinical Management
Rho

Marina Acosta Enslen has 19 years of experience across Phase 2 through 4 studies. She has managed regional and global clinical teams on complex trials, managed clinical teams, developed site and monitor training tools, developed clinical monitoring plans, and successfully delivered operational timelines. Marina has a strong understanding of clinical trial management and delivery requirements that has allowed her to successfully lead teams to meet deliverables.

Missy Lavinder

Senior Project Manager
Rho

Missy has 18 years of clinical research experience as a research coordinator, in-house CRA, study start-up specialist, Clinical Operations Manager and Project Lead. She has experience managing all phases of clinical trials and is experienced in budget management, calculating and tracking site payments, expedited study start-up processes, essential document review, informed consent form review, IRB submissions, overseeing reviews/submissions to Central IRBs, ICH/GCPs, and SOP and procedural document development and review. She has a strong understanding of all aspects of product development which has allowed her to successfully lead teams to meet timeline deliverables for various multi-center trials.

Nick Poulson

Senior Project Manager
Rho

Nick has 8 years of clinical trial experience managing, monitoring, and coordinating Phase 2-4 clinical trials across various therapeutic areas, including pain. He received his doctorate Degree in Cell Biology with a focus on cell division and the cell cycle from Duke University. With this experience also comes expertise in managing at home reported assessments via paper diaries and ePRO devices to ensure timely and accurate reporting by subjects. Additionally, he has a strong understanding of clinical trial management and delivery requirements that has allowed him to successfully lead teams to meet timeline deliverables for various multi-center trials.

NOW AVAILABLE ON-DEMAND

Register now for this webinar