I+D, farmacovigilancia y asuntos reglamentarios

I+D, Farmacovigilancia y Regulatory Affairs

Investigar, desarrollar, probar y lanzar nuevas soluciones farmacológicas. El proceso de desarrollo dura de 8 a 10 años y consta de 4 fases.

  • I+D, Farmacovigilancia y Regulatory Affairs

    Investigar, desarrollar, probar y lanzar nuevas soluciones farmacológicas. El proceso de desarrollo dura de 8 a 10 años y consta de 4 fases.

Título Ubicación Fecha Sort descending Req ID
Restablecer
Modeling & Simulation Scientist
Modeling & Simulation Scientist Parma, IT 23 jun 2025 5264
Parma, IT 23 jun 2025 5264
Regulatory Affairs & Pharmacovigilance Officer Lahore, PK 16 jun 2025 5806
Principal Extractable and Leachable Scientist Parma, IT 15 jun 2025 5557
Regulatory Affairs CMC Specialist - Contract
Regulatory Affairs CMC Specialist - Contract Boston, MA, US 14 jun 2025 5655
Boston, MA, US 14 jun 2025 5655
Real World Evidence Lead Pharmacoepidemiologist
Real World Evidence Lead Pharmacoepidemiologist Europe Remote, IT 13 jun 2025 5661
Europe Remote, IT 13 jun 2025 5661
Senior Clinical Project Manager
Senior Clinical Project Manager Cary, NC, US 13 jun 2025 5797
Cary, NC, US 13 jun 2025 5797
Senior Global Regulatory Affairs Project Manager Parma, IT 11 jun 2025 5787
Clinical Trial Administrator - Maternity leave
Clinical Trial Administrator - Maternity leave Flexible, IT 6 jun 2025 5768
Flexible, IT 6 jun 2025 5768
Clinical Program Leader
Clinical Program Leader Parma, IT 29 may 2025 5447
Parma, IT 29 may 2025 5447
Senior Clinical Research Physician Non-Obstructive Respiratory Diseases Parma, IT 29 may 2025 5448
Clinical Research Physician COPD/Bronchiectasis Parma, IT 29 may 2025 5450