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PAREXEL Strengthens Late Phase and Observational Research Capabilities With Expert Team to Help Biopharma Meet Commercialization Goals
Date:11/23/2011

BOSTON, Nov. 23, 2011 /PRNewswire/ -- PAREXEL International Corporation (NASDAQ: PRXL), a leading global biopharmaceutical services provider, today announced that it has appointed several executives to its global team of late phase and observational research experts in PAREXEL's PACE™ (Peri-Approval Clinical Excellence) group. This team will help sponsors collect the precise data they need to prove the value of their products to multiple stakeholders, and better position their products for commercial success.

"Observational research has become increasingly important as a means to demonstrate product value in a real world clinical setting," said Carol Collins, Ph.D., Corporate Vice President and Worldwide Head of PACE at PAREXEL.

"These appointments to the PAREXEL PACE global team of late phase experts add extensive expertise to help clients optimize the design and execution of their late phase and observational research programs to seamlessly move products from clinical development through commercialization."

The experts newly appointed to PAREXEL's PACE group include:

  • Peggy Schrammel, Vice President and Global Head Portfolio Management, PACE:  Ms. Schrammel's professional experience includes senior-level positions at major clinical research organizations (CROs), where she designed and managed late phase programs including patient registries, clinical-experience trials, pharmacoeconomic trials, and managed-care-based effectiveness trials. Ms. Schrammel received an undergraduate degree in political science and Master of Public Administration from the University of Pittsburgh.
  • Neal Mantick, Senior Director, Global Observational Research'/>"/>

    • SOURCE PAREXEL International Corporation
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