Narcisa Mesaros | VP, Medical Science & Strategy
PPD clinical research business of Thermo Fisher Scientific

Narcisa Mesaros, VP, Medical Science & Strategy, PPD clinical research business of Thermo Fisher Scientific

Narcisa Mesaros, MD, is the Vice President of the Medical Science & Strategy group at PPD, the clinical research business of Thermo Fisher Scientific. She joined PPD from Janssen where she worked as the Clinical Franchise Leader for bacterial vaccines portfolio. Prior, Narcisa spent 15 years at GSK working in positions of increasing responsibility. Narcisa has supported the clinical development of a broad range of vaccines against bacterial and viral pathogens including RSV, COVID-19, and bacterial meningitis. In addition, Narcisa has led the development of combination vaccination products as well as therapeutic vaccine development in oncology. Narcisa has extensive experience with vaccine program design and regulatory interactions, including submission activities, managing key opinion leader (KOL) advisory boards, and independent data monitoring committees (IDMCs). 

Appearances:



Day 2 - Wednesday 30th October @ 13:00

Unlocking the Power of Real-World Data (RWD) and Real-World Evidence (RWE) in Vaccine Development: A Comprehensive Approach to RWE Across the Lifecycle

Regulators and payors are increasingly integrating real-world evidence (RWE) of safety, effectiveness, and value to inform their decision-making.

Discover how RWE, generated using real-world data (RWD), can provide valuable insights from early in development and throughout the vaccine lifecycle.

Join us as we:

  • Explore the diverse types of RWE that can effectively support vaccine development
  • Provide insights into planning for the collection of RWD throughout vaccine development
  • Discuss opportunities to leverage RWD within clinical trials
  • Share examples of uses of RWE from early stage through post-marketing
By considering RWD and RWE early in the development process, manufacturers can optimize integrated evidence generation strategies to expedite vaccine development, approval, and market access.

Key takeaways from the session will include:

-          Understanding how RWD can be used to produce RWE in support of the clinical development and lifecycle of vaccines

-          Recognizing how RWE complements evidence from clinical trials

Identifying challenges and opportunities in planning for RWE generation during vaccine development

last published: 03/Oct/24 13:35 GMT

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