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
Senior Clinical Research Physician Non-Obstructive Respiratory Diseases UK, GB 14 Şub 2026 5448
Intern, Regulatory Affairs, Global Rare Diseases - Summer 2026 Cary, NC, US 14 Şub 2026 6413
Senior Director, Clinical Biometrics & Analytics Parma, IT 12 Şub 2026 6387
Clinical Operations Intern
Clinical Operations Intern Toronto, CA 12 Şub 2026 6934
Toronto, CA 12 Şub 2026 6934
Manager, CMC Regulatory Affairs, Global Rare Diseases Europe, IT 10 Şub 2026 6592
Pharmazeut (all genders) im Praktikum für 2026 / 2027 Hamburg, DE 6 Şub 2026 351
Senior Global Project Manager
Senior Global Project Manager Cary, USA, US 5 Şub 2026 6561
Cary, USA, US 5 Şub 2026 6561
Clinical Program Leader
Clinical Program Leader Europe - Remote, IT 2 Şub 2026 5902
Europe - Remote, IT 2 Şub 2026 5902
Senior Global Project Manager
Senior Global Project Manager Italy, IT 30 Oca 2026 6546
Italy, IT 30 Oca 2026 6546
INTERN - Patient Engagement
INTERN - Patient Engagement PARMA, IT 29 Oca 2026 5993
PARMA, IT 29 Oca 2026 5993
Sr. Director, Clinical Programs, Global Rare Diseases Boston, MA, US 24 Oca 2026 6205
Sr. Manager, CMC Regulatory Affairs
Sr. Manager, CMC Regulatory Affairs United States, US 22 Oca 2026 6204
United States, US 22 Oca 2026 6204
R&D Manufacturing & Technology Transfer Manager Parma, IT 20 Oca 2026 6501
Senior Director, Clinical Excellence AIR - Bronchiectasis & Non-obstructive Lung Diseases Europe, IT 18 Oca 2026 6111
Clinical Trial Documentation & Records Management Lead Parma, IT 17 Oca 2026 6428