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Regulatory Affairs Specialist Project Lead I
4 months ago
Regulatory Affairs Specialist Project Lead I
Location: Bridgewater, NJ (Fully Remote)
Duration: Contract till Oct 2024 with possibility to extend
Fully Remote
This role will require direct experience in US FDA Advisory Committee (ADCOM) Preparation. Experience in Immunology products is preferred, but any ADCOM experience will be considered.
Education and Experience:
• BS/BA degree in a relevant scientific discipline required. Advanced degree (PharmD, PhD, MD or DVM or MSc in Biology, Life Science, or related field) is preferred.
• At least 8-10 years of relevant pharmaceutical/biotechnology experience in R&D, including at least 5 years of relevant Regulatory Affairs experience (regionally and/or global).
