Leads preparation, technical, and regulatory review and finalization of CMC sections for global CTA submissionsTakes a proactive role in the critical review of molecule specific GRA-CMC development strategies and submission content. Makes technical decisions on CMC regulatory issues impacting product submissions across geographies, with support or guidance from Client GRA-CMC regulatory scientists.Provide high quality, timely and clear regulatory advice to allow CMC teams to make well-informed decisionsEvaluate regulatory impact on proposed CMC development plansCommunicates effectively verbally and in writing to influence within GRA-CMC and with CMC development team.Partners with Client GRA CMC (regulatory scientists) develop complex regulatory strategies.Partners with Client RDE (regulatory associates/publishing group) to ensure completion of submission activities.
Job Details
ID | #53488965 |
Estado | Indiana |
Ciudad | Indianapolis |
Tipo de trabajo | Full-time |
Salario | USD TBD TBD |
Fuente | Eurofins |
Showed | 2025-02-19 |
Fecha | 2025-02-19 |
Fecha tope | 2025-04-20 |
Categoría | Etcétera |
Crear un currículum vítae | |
Aplica ya |
Formulation Scientist
Indiana, Indianapolis, 46201 Indianapolis USA