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
Medical Writing Manager
Medical Writing Manager Parma, IT 7 Kas 2025 5903
Parma, IT 7 Kas 2025 5903
Clinical Program Leader
Clinical Program Leader Europe - Remote, IT 7 Kas 2025 5902
Europe - Remote, IT 7 Kas 2025 5902
Statistical Programmer
Statistical Programmer Europe - remote, FR 6 Kas 2025 6151
Europe - remote, FR 6 Kas 2025 6151
EU Regulatory Affairs Manager, Rare Diseases Parma, IT 6 Kas 2025 6145
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
Global Project Lead
Global Project Lead United States, US 5 Kas 2025 6141
United States, US 5 Kas 2025 6141
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
Clinical Trial Administrator - Maternity leave
Clinical Trial Administrator - Maternity leave Flexible, IT 29 Eki 2025 5768
Flexible, IT 29 Eki 2025 5768
Sr. Manager, Regulatory Affairs
Sr. Manager, Regulatory Affairs United States, US 29 Eki 2025 6203
United States, US 29 Eki 2025 6203
Sr. Director, Clinical Programs, Global Rare Diseases Boston, MA, US 29 Eki 2025 6205
Sr. Manager, CMC Regulatory Affairs
Sr. Manager, CMC Regulatory Affairs United States, US 27 Eki 2025 6204
United States, US 27 Eki 2025 6204
Ad Promo Manager, Americas Regulatory Affairs, Global Rare Diseases Boston, MA, US 26 Eki 2025 6005
Preclinical Disease Area Expert
Preclinical Disease Area Expert Parma, IT 25 Eki 2025 4852
Parma, IT 25 Eki 2025 4852
Clinical Program Lead
Clinical Program Lead Cary, NC, US 25 Eki 2025 5950
Cary, NC, US 25 Eki 2025 5950
Senior Director, Global Patient Safety Science
Senior Director, Global Patient Safety Science Everywhere in Europe, IT 24 Eki 2025 6078
Everywhere in Europe, IT 24 Eki 2025 6078
Senior Director, Clinical Excellence AIR - Bronchiectasis & Non-obstructive Lung Diseases Europe, IT 23 Eki 2025 6111
Quality Manager
Quality Manager Vienna, AT 23 Eki 2025 6195
Vienna, AT 23 Eki 2025 6195
Senior Clinical Research Physician Non-Obstructive Respiratory Diseases Parma, IT 21 Eki 2025 5448
Global R&D QA, Senior GMP Product Compliance Specialist Parma, IT 21 Eki 2025 6098
Sr. Director, R&D External Opportunities
Sr. Director, R&D External Opportunities Parma, IT 19 Eki 2025 5830
Parma, IT 19 Eki 2025 5830
Translational and Precision Medicine Lead
Translational and Precision Medicine Lead Europe - remote, GB 15 Eki 2025 6152
Europe - remote, GB 15 Eki 2025 6152