16.05.24 | Vollzeit | Offenbach am Main | BioNTech SERegulatory specialists, and program managers as well as diagnostic partners. You will play a vital role in the planning, execution, and management of clinical trials for medical devices and IVDs. Independently coordinate IVD and/or companion diagnostics (CDx) Co-development projects as SME. Contribute
Später ansehen16.05.24 | Vollzeit | Ludwigshafen am Rhein | BioNTech SERegulatory specialists, and program managers as well as diagnostic partners. You will play a vital role in the planning, execution, and management of clinical trials for medical devices and IVDs. Independently coordinate IVD and/or companion diagnostics (CDx) Co-development projects as SME. Contribute
Später ansehen16.05.24 | Vollzeit | Darmstadt | BioNTech SERegulatory specialists, and program managers as well as diagnostic partners. You will play a vital role in the planning, execution, and management of clinical trials for medical devices and IVDs. Independently coordinate IVD and/or companion diagnostics (CDx) Co-development projects as SME. Contribute
Später ansehen16.05.24 | Vollzeit | Kaiserslautern | BioNTech SERegulatory specialists, and program managers as well as diagnostic partners. You will play a vital role in the planning, execution, and management of clinical trials for medical devices and IVDs. Independently coordinate IVD and/or companion diagnostics (CDx) Co-development projects as SME. Contribute
Später ansehen16.05.24 | Vollzeit | Mannheim | BioNTech SERegulatory specialists, and program managers as well as diagnostic partners. You will play a vital role in the planning, execution, and management of clinical trials for medical devices and IVDs. Independently coordinate IVD and/or companion diagnostics (CDx) Co-development projects as SME. Contribute
Später ansehen16.05.24 | Vollzeit | Kaiserslautern | BioNTech SERegulatory specialists, and program managers as well as diagnostic partners. You will play a vital role in the planning, execution, and management of clinical trials for medical devices and IVDs. Independently coordinate IVD and/or companion diagnostics (CDx) Co-development projects as SME. Contribute
Später ansehen16.05.24 | Vollzeit | Ludwigshafen am Rhein | BioNTech SERegulatory specialists, and program managers as well as diagnostic partners. You will play a vital role in the planning, execution, and management of clinical trials for medical devices and IVDs. Independently coordinate IVD and/or companion diagnostics (CDx) Co-development projects as SME. Contribute
Später ansehen16.05.24 | Vollzeit | Hanau | BioNTech SERegulatory specialists, and program managers as well as diagnostic partners. You will play a vital role in the planning, execution, and management of clinical trials for medical devices and IVDs. Independently coordinate IVD and/or companion diagnostics (CDx) Co-development projects as SME. Contribute
Später ansehen08.05.24 | Vollzeit | Freising | Daiichi Sankyo Europe GmbHRisk Management, Signal Detection, and medical review of ICSRs). Reporting Reports to the European Senior Director Oncology Value, Access & Pricing Co-leads DSE CSPV Specialty Medicines product team to manage safety profiles of assigned assets with oversight of junior physicians or scientists
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