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
Patient Safety Science Lead
Patient Safety Science Lead Parma, IT 24 Tem 2026 7546
Parma, IT 24 Tem 2026 7546
Head of Clinical Project Management
Head of Clinical Project Management Italy, IT 23 Tem 2026 7386
Italy, IT 23 Tem 2026 7386
INTERN - Patient Engagement
INTERN - Patient Engagement PARMA, IT 22 Tem 2026 5993
PARMA, IT 22 Tem 2026 5993
Clinical Research Physician, Global Rare Diseases
Clinical Research Physician, Global Rare Diseases Europe - Remote, IT 22 Tem 2026 7356
Europe - Remote, IT 22 Tem 2026 7356
INTERN -R&D Assistant
INTERN -R&D Assistant Parma, IT 22 Tem 2026 7418
Parma, IT 22 Tem 2026 7418
Senior Manager, CMC Regulatory Affairs, Global Rare Diseases Cary, NC, US 22 Tem 2026 7551
R&D Process Excellence & Digital Solutions Senior Manager Parma, IT 19 Tem 2026 7313
TESISTA - Digitalizzazione dei processi di laboratorio Parma, IT 17 Tem 2026 7305
Senior Manager, CMC Regulatory Affairs, Global Rare Diseases Parma, IT 17 Tem 2026 7394
Clinical Operations Lead
Clinical Operations Lead Italy remote, IT 17 Tem 2026 7376
Italy remote, IT 17 Tem 2026 7376
Senior Global Patient Safety Physician
Senior Global Patient Safety Physician Europe, remote, IT 17 Tem 2026 7401
Europe, remote, IT 17 Tem 2026 7401
R&D Data Visualization Engineer
R&D Data Visualization Engineer Parma, IT 17 Tem 2026 7301
Parma, IT 17 Tem 2026 7301
Manager, Americas Regulatory Affairs Labeling & Promotion, Global Rare Diseases Boston, MA, US 17 Tem 2026 7526
Clinical Innovation Project Manager
Clinical Innovation Project Manager Italy, IT 14 Tem 2026 7388
Italy, IT 14 Tem 2026 7388
Medical Information & PV Officer
Medical Information & PV Officer Zaventem (BE) or Schiphol (NL), BE 14 Tem 2026 7089
Zaventem (BE) or Schiphol (NL), BE 14 Tem 2026 7089
Senior Director, Clinical Excellence AIR - Bronchiectasis & Non-obstructive Lung Diseases Europe, IT 11 Tem 2026 6111
Specialist, Labelling & Compliance Regulatory Affairs, Global Rare Diseases Parma, IT 11 Tem 2026 7364
Senior Clinical Project Manager
Senior Clinical Project Manager Italy, IT 11 Tem 2026 7374
Italy, IT 11 Tem 2026 7374
Manager, EU & International Regulatory Affairs, Global Rare Diseases Dublin, IE 11 Tem 2026 7302
R&D Bioinformatician Lead
R&D Bioinformatician Lead Parma, IT 10 Tem 2026 7280
Parma, IT 10 Tem 2026 7280
Principal Regulatory Writer, Global Rare Diseases Parma, IT 10 Tem 2026 7341
Statistical Programmer
Statistical Programmer Parma, IT 8 Tem 2026 7444
Parma, IT 8 Tem 2026 7444
Senior Director, Clinical Biometrics & Analytics Parma, IT 7 Tem 2026 6387
PSMF & Compliance Manager
PSMF & Compliance Manager Parma, IT 7 Tem 2026 7452
Parma, IT 7 Tem 2026 7452
Specialist Care Therapeutic Area, Global Regulatory Affairs and Patient Safety - Temporary Paris, Bois Colombes, FR 7 Tem 2026 7450