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 21 arasındaki sonuçlar - 21
Başlık Konum Sort descending Tarih Req ID
Sıfırla
Lead Clinical Research Associate
Lead Clinical Research Associate UK/France, IT 11 Nis 2024 3504
UK/France, IT 11 Nis 2024 3504
Global Project Manager
Global Project Manager Stockholm, IT 12 Nis 2024 3490
Stockholm, IT 12 Nis 2024 3490
Senior DP Analytical Scientist
Senior DP Analytical Scientist Parma, IT 18 Mar 2024 3834
Parma, IT 18 Mar 2024 3834
Real World Evidence Study Manager - Temporary Parma, IT 4 Nis 2024 3946
Pharmacovigilance Specialist
Pharmacovigilance Specialist Parma, IT 11 Nis 2024 3596
Parma, IT 11 Nis 2024 3596
Rare Disease Clinical Project Manager
Rare Disease Clinical Project Manager Parma, IT 29 Mar 2024 3809
Parma, IT 29 Mar 2024 3809
Drug Substance Analytical Lead
Drug Substance Analytical Lead Parma or anywhere in Europe, IT 5 Nis 2024 2942
Parma or anywhere in Europe, IT 5 Nis 2024 2942
Clinical Project Manager
Clinical Project Manager Paris, Bois Colombes, FR 13 Nis 2024 3823
Paris, Bois Colombes, FR 13 Nis 2024 3823
R&D Global Project Leader - Rare Diseases
R&D Global Project Leader - Rare Diseases Global - Remote, IT 26 Mar 2024 3402
Global - Remote, IT 26 Mar 2024 3402
Clinical Research Physician
Clinical Research Physician Europe - remote, IT 27 Mar 2024 3609
Europe - remote, IT 27 Mar 2024 3609
Rare Disease Clinical Research Physician
Rare Disease Clinical Research Physician Europe - remote, IT 26 Mar 2024 3507
Europe - remote, IT 26 Mar 2024 3507
Global Regulatory Project Specialist
Global Regulatory Project Specialist Cary, NC, US 20 Mar 2024 3810
Cary, NC, US 20 Mar 2024 3810
Global Regulatory Project Specialist
Global Regulatory Project Specialist Cary, NC, US 20 Mar 2024 3810
Cary, NC, US 20 Mar 2024 3810
Regulatory Affairs Specialist, Rare Diseases
Regulatory Affairs Specialist, Rare Diseases Cary, NC, US 1 Nis 2024 3928
Cary, NC, US 1 Nis 2024 3928
Assoc Director, Advertising and Promotion, Commercial Labeling Lead, Americas Reg Affairs, GRD Cary, NC, US 28 Mar 2024 3804
Clinical Project Manager
Clinical Project Manager Cary, NC, US 11 Nis 2024 3806
Cary, NC, US 11 Nis 2024 3806
Global RA Labeling Unit Head
Global RA Labeling Unit Head Cary, NC, US 10 Nis 2024 3978
Cary, NC, US 10 Nis 2024 3978
Pharmaceutical Affairs Officer
Pharmaceutical Affairs Officer Brussels, BE 20 Mar 2024 3883
Brussels, BE 20 Mar 2024 3883
PV/QA & Specialist
PV/QA & Specialist Bratislava, SK 3 Nis 2024 3936
Bratislava, SK 3 Nis 2024 3936
eTMF Specialist
eTMF Specialist Boston, MA, US 13 Nis 2024 3557
Boston, MA, US 13 Nis 2024 3557
Regulatory Affairs Trainee
Regulatory Affairs Trainee Barcelona, ES 5 Nis 2024 3783
Barcelona, ES 5 Nis 2024 3783