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
Regulatory Affairs & Pharmacovigilance Officer Lahore, PK 16 Haz 2025 5806
Principal Extractable and Leachable Scientist Parma, IT 15 Haz 2025 5557
Regulatory Affairs CMC Specialist - Contract
Regulatory Affairs CMC Specialist - Contract Boston, MA, US 14 Haz 2025 5655
Boston, MA, US 14 Haz 2025 5655
Real World Evidence Lead Pharmacoepidemiologist
Real World Evidence Lead Pharmacoepidemiologist Europe Remote, IT 13 Haz 2025 5661
Europe Remote, IT 13 Haz 2025 5661
Senior Clinical Project Manager
Senior Clinical Project Manager Cary, NC, US 13 Haz 2025 5797
Cary, NC, US 13 Haz 2025 5797
Senior Global Regulatory Affairs Project Manager Parma, IT 11 Haz 2025 5787
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
Modeling & Simulation Scientist
Modeling & Simulation Scientist Parma, IT 25 May 2025 5264
Parma, IT 25 May 2025 5264