21.03.24 | Vollzeit | Hamburg | Advanced Resource ManagersNew Drug Application (BLA/NDA), Investigational Medicinal Product Dossier (IMPD), and Investigational New Drug (IND). Conduct gap analyses of client-provided packages, identifying critical CMC development issues and devising strategies for resolution. Support due diligence processes and prepare
Später ansehen21.03.24 | Vollzeit | Hamburg | Advanced Resource ManagersLicense Application/New Drug Application (BLA/NDA), Investigational Medicinal Product Dossier (IMPD), and Investigational New Drug (IND). Conduct gap analyses of client-provided packages, identifying critical CMC development issues and devising strategies for resolution. Support due diligence processes
Später ansehen14.04.24 | Vollzeit | Bremen | Advanced Resource ManagersExpectations, and facilitating the approval of regulatory submissions. Prepare quality sections for Marketing Authorisation Applications (MAA), Biologics License Application/New Drug Application (BLA/NDA), Investigational Medicinal Product Dossier (IMPD), and Investigational New Drug (IND). Conduct gap
Später ansehen14.04.24 | Vollzeit | Düsseldorf | Advanced Resource ManagersAnd facilitating the approval of regulatory submissions. Prepare quality sections for Marketing Authorisation Applications (MAA), Biologics License Application/New Drug Application (BLA/NDA), Investigational Medicinal Product Dossier (IMPD), and Investigational New Drug (IND). Conduct gap analyses of client
Später ansehen14.04.24 | Vollzeit | Stuttgart | Advanced Resource ManagersAnd facilitating the approval of regulatory submissions. Prepare quality sections for Marketing Authorisation Applications (MAA), Biologics License Application/New Drug Application (BLA/NDA), Investigational Medicinal Product Dossier (IMPD), and Investigational New Drug (IND). Conduct gap analyses of client
Später ansehen11.04.24 | Vollzeit | München | Advanced Resource ManagersExpectations, and facilitating the approval of regulatory submissions. Prepare quality sections for Marketing Authorisation Applications (MAA), Biologics License Application/New Drug Application (BLA/NDA), Investigational Medicinal Product Dossier (IMPD), and Investigational New Drug (IND). Conduct gap
Später ansehen11.04.24 | Vollzeit | München | Advanced Resource ManagersAnd facilitating the approval of regulatory submissions. Prepare quality sections for Marketing Authorisation Applications (MAA), Biologics License Application/New Drug Application (BLA/NDA), Investigational Medicinal Product Dossier (IMPD), and Investigational New Drug (IND). Conduct gap analyses of client
Später ansehen21.03.24 | Vollzeit | Hamburg | Advanced Resource ManagersLicense Application/New Drug Application (BLA/NDA), Investigational Medicinal Product Dossier (IMPD), and Investigational New Drug (IND). Conduct gap analyses of client-provided packages, identifying critical CMC development issues and devising strategies for resolution. Support due diligence processes
Später ansehen21.03.24 | Vollzeit | Hamburg | Advanced Resource ManagersNew Drug Application (BLA/NDA), Investigational Medicinal Product Dossier (IMPD), and Investigational New Drug (IND). Conduct gap analyses of client-provided packages, identifying critical CMC development issues and devising strategies for resolution. Support due diligence processes and prepare
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