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.
Arama terimi "". Sayfa 1/1, 1 ile 19 arasındaki sonuçlar - 19
Başlık Konum Tarih Sort descending Req ID
Sıfırla
Senior Global Regulatory Affairs Manager
Senior Global Regulatory Affairs Manager Parma, IT 29 Oca 2025 5131
Parma, IT 29 Oca 2025 5131
Clinical Project Manager
Clinical Project Manager Paris, Bois Colombes, FR 28 Oca 2025 3823
Paris, Bois Colombes, FR 28 Oca 2025 3823
Trainee Medical Affairs (BU Special Care)
Trainee Medical Affairs (BU Special Care) Barcelona, ES 28 Oca 2025 5117
Barcelona, ES 28 Oca 2025 5117
Preclinical Bioinformatics Lead
Preclinical Bioinformatics Lead Europe - remote, SE 23 Oca 2025 4522
Europe - remote, SE 23 Oca 2025 4522
Global Regulatory Affairs Labeling & Promotional Manager
Global Regulatory Affairs Labeling & Promotional Manager Cary, NC, US 23 Oca 2025 5112
Cary, NC, US 23 Oca 2025 5112
Manager, Regulatory Affairs Operations, Rare Diseases
Manager, Regulatory Affairs Operations, Rare Diseases Boston, MA, US 23 Oca 2025 5114
Boston, MA, US 23 Oca 2025 5114
Intern, Global Rare Diseases Clinical Trial Administrator - Summer 2025
Intern, Global Rare Diseases Clinical Trial Administrator - Summer 2025 Cary, NC, US 22 Oca 2025 4967
Cary, NC, US 22 Oca 2025 4967
Intern, Global Pipeline Strategy - Summer 2025
Intern, Global Pipeline Strategy - Summer 2025 Boston, MA, US 22 Oca 2025 4969
Boston, MA, US 22 Oca 2025 4969
Site Engagement Lead
Site Engagement Lead Cary, NC, US 22 Oca 2025 5043
Cary, NC, US 22 Oca 2025 5043
Site Engagement Lead
Site Engagement Lead Cary, NC, US 22 Oca 2025 5044
Cary, NC, US 22 Oca 2025 5044
Real World Evidence Study Manager - Temporary
Real World Evidence Study Manager - Temporary Parma, IT 21 Oca 2025 3946
Parma, IT 21 Oca 2025 3946
Global R&D Department Assistant
Global R&D Department Assistant Parma, IT 21 Oca 2025 5077
Parma, IT 21 Oca 2025 5077
Head of Global Pharmacovigilance Center of Excellence
Head of Global Pharmacovigilance Center of Excellence Parma, IT 15 Oca 2025 4856
Parma, IT 15 Oca 2025 4856
Global Regulatory Affairs Manager
Global Regulatory Affairs Manager Parma, IT 14 Oca 2025 4978
Parma, IT 14 Oca 2025 4978
Intern, Regulatory Affairs - Summer 2025
Intern, Regulatory Affairs - Summer 2025 Cary, NC, US 14 Oca 2025 5003
Cary, NC, US 14 Oca 2025 5003
Clinical Risk Operation Specialist
Clinical Risk Operation Specialist Parma, IT 11 Oca 2025 4979
Parma, IT 11 Oca 2025 4979
Manager, Regulatory Affairs Operations, Rare Diseases
Manager, Regulatory Affairs Operations, Rare Diseases Boston, MA, US 10 Oca 2025 5029
Boston, MA, US 10 Oca 2025 5029
Pharmazeut (all genders) im Praktikum für 2025 / 2026
Pharmazeut (all genders) im Praktikum für 2025 / 2026 Hamburg, DE 2 Oca 2025 351
Hamburg, DE 2 Oca 2025 351
DS Analytical Technician
DS Analytical Technician Parma, IT 2 Ara 2024 4553
Parma, IT 2 Ara 2024 4553