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Consultant - Regulatory Affairs, NJ
Seeking Regulatory Affairs position where 20+ years of experience in pharmaceuticals Regulatory Affairs and R&D will add value.
Clinical Regulatory Affairs
About Me
Industry: |
Science & Biotech |
|---|---|
Occupation: |
Clinical Regulatory Affairs |
Education level: |
Doctorate |
Will Relocate: |
Yes |
Location: |
Westfield, NJ |
Keywords
RAC Certification, Microbiology and fermentation, toxicity assays high-throughput screening, CMC, project and staff management, submissions, compliance, IND NDA submissions, Consultant, molecular microbiologist, toxicity assays , project management, submissions, compliance, IND/NDA/eCTD, regulatory, pharmaceuticals, regulatory scientist
