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
Sr. Manager, CMC Regulatory Affairs
Sr. Manager, CMC Regulatory Affairs United States, US 20 feb 2026 6204
United States, US 20 feb 2026 6204
Clinical Program Leader, Neonatology & Care
Clinical Program Leader, Neonatology & Care Europe, IT 19 feb 2026 6955
Europe, IT 19 feb 2026 6955
R&D Manufacturing & Technology Transfer Manager Parma, IT 18 feb 2026 6501
Senior Director, Clinical Excellence AIR - Bronchiectasis & Non-obstructive Lung Diseases Europe, IT 16 feb 2026 6111
Clinical Trial Documentation & Records Management Lead Parma, IT 15 feb 2026 6428
Senior Clinical Research Physician Non-Obstructive Respiratory Diseases UK, GB 14 feb 2026 5448
Intern, Regulatory Affairs, Global Rare Diseases - Summer 2026 Cary, NC, US 14 feb 2026 6413
Senior Director, Clinical Biometrics & Analytics Parma, IT 12 feb 2026 6387
Manager, CMC Regulatory Affairs, Global Rare Diseases Europe, IT 10 feb 2026 6592
Pharmazeut (all genders) im Praktikum für 2026 / 2027 Hamburg, DE 6 feb 2026 351
Senior Global Project Manager
Senior Global Project Manager Cary, USA, US 5 feb 2026 6561
Cary, USA, US 5 feb 2026 6561
Clinical Program Leader
Clinical Program Leader Europe - Remote, IT 2 feb 2026 5902
Europe - Remote, IT 2 feb 2026 5902
Senior Global Project Manager
Senior Global Project Manager Italy, IT 30 ene 2026 6546
Italy, IT 30 ene 2026 6546
INTERN - Patient Engagement
INTERN - Patient Engagement PARMA, IT 29 ene 2026 5993
PARMA, IT 29 ene 2026 5993