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 ascending Req ID
Sıfırla
Pharmazeut (all genders) im Praktikum für 2027 Hamburg, DE 4 May 2026 351
Pharmaceutical Affairs Manager | All genders | Full-time Vienna, AT 5 May 2026 7255
Senior Manager, CMC Regulatory Affairs, Global Rare Diseases Europe, IT 8 May 2026 6592
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
R&D Bioinformatician Lead
R&D Bioinformatician Lead Parma, IT 13 May 2026 7280
Parma, IT 13 May 2026 7280
INTERN - Clinical Supply Management & Distribution Parma, IT 13 May 2026 7186
Senior Director, Clinical Excellence AIR - Bronchiectasis & Non-obstructive Lung Diseases Europe, IT 14 May 2026 6111
Translational and Precision Medicine Lead 1
Translational and Precision Medicine Lead 1 Europe - remote, GB 15 May 2026 7208
Europe - remote, GB 15 May 2026 7208
R&D Data Visualization Engineer
R&D Data Visualization Engineer Parma, IT 19 May 2026 7301
Parma, IT 19 May 2026 7301
TESISTA - Digitalizzazione dei processi di laboratorio Parma, IT 20 May 2026 7305
INTERN - Patient Engagement
INTERN - Patient Engagement PARMA, IT 25 May 2026 5993
PARMA, IT 25 May 2026 5993
Global Pharmacovigilance Medical Safety Writer - Temporary Parma, IT 27 May 2026 7237
Head of Biologic Drug Substance - Process & Analytical Development Parma, IT 29 May 2026 7233