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
INTERN - Clinical Supply Management & Distribution Parma, IT 13 may 2026 7186
R&D Bioinformatician Lead
R&D Bioinformatician Lead Parma, IT 13 may 2026 7280
Parma, IT 13 may 2026 7280
Clinical Program Leader
Clinical Program Leader Cary, NC, US 10 may 2026 7017
Cary, NC, US 10 may 2026 7017
Master's thesis in computational modelling of aerosol deposition in respiratory system Parma, IT 10 may 2026 6598
Senior Director, Clinical Biometrics & Analytics Parma, IT 10 may 2026 6387
Regulatory Affairs Specialist
Regulatory Affairs Specialist Barcelona, ES 10 may 2026 6966
Barcelona, ES 10 may 2026 6966
Senior Manager, CMC Regulatory Affairs, Global Rare Diseases Europe, IT 8 may 2026 6592
Pharmaceutical Affairs Manager | All genders | Full-time Vienna, AT 5 may 2026 7255
Pharmazeut (all genders) im Praktikum für 2026 / 2027 Hamburg, DE 4 may 2026 351
Head of Biologic Drug Substance - Process & Analytical Development Parma, IT 30 abr 2026 7233
Global Pharmacovigilance Medical Safety Writer - Temporary Parma, IT 28 abr 2026 7237
INTERN - Patient Engagement
INTERN - Patient Engagement PARMA, IT 26 abr 2026 5993
PARMA, IT 26 abr 2026 5993
Translational and Precision Medicine Lead 1
Translational and Precision Medicine Lead 1 Europe - remote, GB 16 abr 2026 7208
Europe - remote, GB 16 abr 2026 7208
Senior Director, Clinical Excellence AIR - Bronchiectasis & Non-obstructive Lung Diseases Europe, IT 15 abr 2026 6111