18.04.24 | Vollzeit | Frankfurt am Main | Exact SciencesData from conferences and literature, as well as competitive intelligence, and report back on findings to medical affairs and marketing stakeholders. - Pipeline & Clinical Trials Support - Identify physicians currently managing patients with breast and colorectal cancer and cultivate a network
Später ansehen08.04.24 | Vollzeit | Kaiserslautern | BioNTech SEAnd contribution to required documents (e.g. risk analysis, briefing books, IND, IMPD, study plans and reports, etc.) in close collaboration with Technical and Regulatory Affairs teams Act as point of contact for CMOs and analytical laboratories for GMP manufacturing and quality control, to ensure the supply
Später ansehen08.04.24 | Vollzeit | Kaiserslautern | BioNTech SEAnd contribution to required documents (e.g. risk analysis, briefing books, IND, IMPD, study plans and reports, etc.) in close collaboration with Technical and Regulatory Affairs teams Act as point of contact for CMOs and analytical laboratories for GMP manufacturing and quality control, to ensure the supply
Später ansehen08.04.24 | Vollzeit | Kaiserslautern | BioNTech SEAnd contribution to required documents (e.g. risk analysis, briefing books, IND, IMPD, study plans and reports, etc.) in close collaboration with Technical and Regulatory Affairs teams Act as point of contact for CMOs and analytical laboratories for GMP manufacturing and quality control, to ensure the supply
Später ansehen08.04.24 | Vollzeit | Kaiserslautern | BioNTech SEAnd contribution to required documents (e.g. risk analysis, briefing books, IND, IMPD, study plans and reports, etc.) in close collaboration with Technical and Regulatory Affairs teams Act as point of contact for CMOs and analytical laboratories for GMP manufacturing and quality control, to ensure the supply
Später ansehen08.04.24 | Vollzeit | Kaiserslautern | BioNTech SEAnd contribution to required documents (e.g. risk analysis, briefing books, IND, IMPD, study plans and reports, etc.) in close collaboration with Technical and Regulatory Affairs teams Act as point of contact for CMOs and analytical laboratories for GMP manufacturing and quality control, to ensure the supply
Später ansehen08.04.24 | Vollzeit | Kaiserslautern | BioNTech SEAnd contribution to required documents (e.g. risk analysis, briefing books, IND, IMPD, study plans and reports, etc.) in close collaboration with Technical and Regulatory Affairs teams Act as point of contact for CMOs and analytical laboratories for GMP manufacturing and quality control, to ensure the supply
Später ansehen08.04.24 | Vollzeit | Kaiserslautern | BioNTech SEAnd contribution to required documents (e.g. risk analysis, briefing books, IND, IMPD, study plans and reports, etc.) in close collaboration with Technical and Regulatory Affairs teams Act as point of contact for CMOs and analytical laboratories for GMP manufacturing and quality control, to ensure the supply
Später ansehen08.04.24 | Vollzeit | Kaiserslautern | BioNTech SEAnd contribution to required documents (e.g. risk analysis, briefing books, IND, IMPD, study plans and reports, etc.) in close collaboration with Technical and Regulatory Affairs teams Act as point of contact for CMOs and analytical laboratories for GMP manufacturing and quality control, to ensure the supply
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