Myra Herrle's Location

Glenview, Illinois, United States

Myra Herrle's Work

  • Executive Vice President Regulatory Affairs @ POINT Biopharma
  • Vice President Regulatory Affairs @ GlycoMimetics
  • Senior Director Regulatory Therapeutic Head Oncology US and Canada and Affiliates @ AbbVie
  • Senior Global Program Regulatory Director Critical Care Drug Regulatory Affairs @ Novartis
  • Global Therapeutic Area Lead and Executive Director Dra @ Novartis
  • Global Program Regulatory Director, Respiratory Dra @ Novartis
  • Scientific Officer, Scientific Review Committee @ Novartis
  • Senior Associate Director and Associate Director Oncology Dra @ Novartis
  • Director Oncology, Musculoskeletal, Inflammatory Diseases @ GSK
  • Principal and Senior Clinical Research Scientist @ GSK

Myra Herrle's Education

  • University of Oklahoma Health Sciences Center

    Doctor of Philosophy (Microbiology, Immunology)

    1982 - 1987
  • Kerala University, Thiruvananthapuram

    Bachelor of Science (Pharmacy)

    1977 - 1982

Myra Herrle's Skills

  • Drug Development
  • FDA
  • NDA
  • IND
  • Oncology
  • FDA Advisory Committee
  • FDA Breakthrough designation
  • Expanded Access
  • Protocol Design
  • Clinical Development

Myra Herrle's Summary

Myra Herrle, based in Glenview, Illinois, United States, is currently a Executive Vice President Regulatory Affairs at Point Biopharma, bringing experience from previous roles at Glycomimetics, Abbvie and Novartis. Myra Herrle holds a 1982 - 1987 Doctor of Philosophy in Microbiology, Immunology @ University of Oklahoma Health Sciences Center. With a robust skill set that includes Drug Development, FDA, NDA, IND, Oncology and more, Myra Herrle contributes valuable insights to the industry. Myra Herrle has 5 emails and 2 mobile phone numbers on RocketReach.

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