Susan Way
Senior Vice President, Drug Development & Regulatory Affairs
- Role
- Executive Vice President Program Management at Neurotrauma Sciences, Llc
- Location
- Danbury, CT, US
- LinkedIn followers
- 500 followers
About Susan Way
Senior Vice President Drug Development and Regulatory Affairs: 30 years\' experience with a demonstrated history of working in the pharma/biotechnology industry. Strong technical background, as well as expertise in program/project management, drug development, clinical development, biotechnology, drug-device combination products, regulatory submissions (INDs, NDAs, CTAs), U.S. Food and Drug Administration (FDA), Research and Development (R&D) and Life Sciences. Extensive experience in cross-functional leadership and strategic planning.
Experience
Executive Vice President Program Management
Jul 2024 — Present · Alpharetta, GA, US
Education
University of Kentucky College of Pharmacy
Doctor of Philosophy - PhD, Pharmaceutical Sciences
Skills
- U.s. Food and Drug Administration (Fda)
- Assay Development
- Glp
- Technology Transfer
- Life Sciences
- Ctms
- Good Laboratory Practice (Glp)
- Pharmaceutics
- Drug Discovery
- Regulatory Affairs
- Lifesciences
- CRO
- Infectious Diseases
- R&D
- Clinical Trials
- Gmp
- Biotechnology
- Research and Development (R&D)
- Project Management
- Clinical Development
- Formulation
- Drug Development
- Regulatory Submissions
- Validation
- Gcp
- Biopharmaceuticals
- Pharmaceutical Industry
- Sop
- Fda
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