CSV Engineer
documentation and activities comply with FDA, EMA, and other relevant regulatory standards (e.g., 21 CFR Part 11, GxP). Conduct...
Lugar: Warren, NJ | 07/11/2024 18:11:12 PM | Salario: S/. No Especificado | Empresa: Azzur Group
documentation and activities comply with FDA, EMA, and other relevant regulatory standards (e.g., 21 CFR Part 11, GxP). Conduct...
for an industry Sponsor or CRO or ARO managing FDA and/or EMA-regulated clinical trials. Extensive experience in all facets of study... Development, Medrio, REDCap, etc.) Required Skill/Ability 4: Comprehensive technical knowledge of FDA and EMA clinical data...