R&D, Pharmacovigilance & Regulatory Affairs_tr

Ar-Ge, Farmakovijilans ve Ruhsatlandırma İşleri

Yeni ilaç çözümleri araştırma, geliştirme, test etme ve piyasaya sürme. Geliştirme süreci 8 ila 10 yıl sürer ve 4 fazdan oluşur.

  • Ar-Ge, Farmakovijilans ve Ruhsatlandırma İşleri

    Yeni ilaç çözümleri araştırma, geliştirme, test etme ve piyasaya sürme. Geliştirme süreci 8 ila 10 yıl sürer ve 4 fazdan oluşur.

Başlık Konum Tarih Sort descending Req ID
Sıfırla
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
CSV Specialist
CSV Specialist Parma, IT 29 May 2025 5473
Parma, IT 29 May 2025 5473
Scientific Knowledge - Respiratory Unit Head Parma, IT 27 May 2025 5686
Modeling & Simulation Scientist
Modeling & Simulation Scientist Parma, IT 25 May 2025 5264
Parma, IT 25 May 2025 5264
Process Development Scientist
Process Development Scientist Parma, IT 24 May 2025 5446
Parma, IT 24 May 2025 5446
Principal Extractable and Leachable Scientist Parma, IT 17 May 2025 5557
Manager Information & Regulatory Affairs (all genders) Hamburg, DE 16 May 2025 5214
Regulatory Affairs CMC Specialist - Contract
Regulatory Affairs CMC Specialist - Contract Boston, MA, US 16 May 2025 5655
Boston, MA, US 16 May 2025 5655
Real World Evidence Lead Pharmacoepidemiologist
Real World Evidence Lead Pharmacoepidemiologist Europe Remote, IT 15 May 2025 5661
Europe Remote, IT 15 May 2025 5661
Technical Affairs Trainee
Technical Affairs Trainee Barcelona, ES 14 May 2025 5652
Barcelona, ES 14 May 2025 5652
Global Pharmacovigilance Operations Manager, Care Parma, IT 8 May 2025 5175
INTERN - Medicinal Chemistry Lab Technician Parma, IT 3 May 2025 5485