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
Sr. Director, Clinical Programs, Global Rare Diseases
Sr. Director, Clinical Programs, Global Rare Diseases Boston, MA, US 27 Kas 2025 6205
Boston, MA, US 27 Kas 2025 6205
Sr. Manager, Regulatory Affairs
Sr. Manager, Regulatory Affairs United States, US 27 Kas 2025 6203
United States, US 27 Kas 2025 6203
Clinical Pharmacologist Lead
Clinical Pharmacologist Lead Parma, IT 26 Kas 2025 6307
Parma, IT 26 Kas 2025 6307
Sr. Manager, CMC Regulatory Affairs
Sr. Manager, CMC Regulatory Affairs United States, US 25 Kas 2025 6204
United States, US 25 Kas 2025 6204
Ad Promo Manager, Americas Regulatory Affairs, Global Rare Diseases
Ad Promo Manager, Americas Regulatory Affairs, Global Rare Diseases Boston, MA, US 24 Kas 2025 6005
Boston, MA, US 24 Kas 2025 6005
Senior Analytical Scientist Biologics
Senior Analytical Scientist Biologics Parma, IT 24 Kas 2025 6192
Parma, IT 24 Kas 2025 6192
Senior Director, Global Patient Safety Science
Senior Director, Global Patient Safety Science Everywhere in Europe, IT 22 Kas 2025 6078
Everywhere in Europe, IT 22 Kas 2025 6078
Senior Director, Clinical Excellence AIR - Bronchiectasis & Non-obstructive Lung Diseases
Senior Director, Clinical Excellence AIR - Bronchiectasis & Non-obstructive Lung Diseases Europe, IT 21 Kas 2025 6111
Europe, IT 21 Kas 2025 6111
Senior Clinical Research Physician Non-Obstructive Respiratory Diseases
Senior Clinical Research Physician Non-Obstructive Respiratory Diseases Parma, IT 19 Kas 2025 5448
Parma, IT 19 Kas 2025 5448
Global R&D QA, Senior GMP Product Compliance Specialist
Global R&D QA, Senior GMP Product Compliance Specialist Parma, IT 19 Kas 2025 6098
Parma, IT 19 Kas 2025 6098
Translational and Precision Medicine Lead
Translational and Precision Medicine Lead Europe - remote, GB 13 Kas 2025 6152
Europe - remote, GB 13 Kas 2025 6152
Clinical Program Leader
Clinical Program Leader Europe - Remote, IT 7 Kas 2025 5902
Europe - Remote, IT 7 Kas 2025 5902
EU Regulatory Affairs Manager, Rare Diseases
EU Regulatory Affairs Manager, Rare Diseases Parma, IT 6 Kas 2025 6145
Parma, IT 6 Kas 2025 6145
Global Project Lead
Global Project Lead United States, US 5 Kas 2025 6141
United States, US 5 Kas 2025 6141
Clinical Program Leader, R&D Global Rare Diseases
Clinical Program Leader, R&D Global Rare Diseases Europe - remote, GB 5 Kas 2025 6146
Europe - remote, GB 5 Kas 2025 6146
CMC Technical Leader
CMC Technical Leader Europe - remote / US - remote, IT 4 Kas 2025 6137
Europe - remote / US - remote, IT 4 Kas 2025 6137
INTERN - Process Technologist
INTERN - Process Technologist Parma, IT 4 Kas 2025 6228
Parma, IT 4 Kas 2025 6228
INTERN - Patient Engagement
INTERN - Patient Engagement PARMA, IT 3 Kas 2025 5993
PARMA, IT 3 Kas 2025 5993