05.06.24 | Vollzeit | Ludwigshafen am Rhein | AbbVie Deutschland GmbH & Co. KGInvestigational products (pharmaceutical drug products as well as drug - device combination products), testing, and related documents Manages a quality organization of up to 5 direct reports and up to 50 total QA department members. Directly responsible for the effective organization, administration, training
Später ansehen05.06.24 | Vollzeit | Ludwigshafen am Rhein | JobLeads GmbH | 100.000 € - 125.000 € Of clinical trial supplies, including API/drug substance, ingredients, bulk drug product and finished investigational products (pharmaceutical drug products as well as drug/device combination products), testing, and related documents. - Manages a quality organization of up to 5 direct reports and up to 50
Später ansehen06.06.24 | Vollzeit | Kaiserslautern | BioNTech SEFor all statistical aspects Serve as the biostatistics lead core team member for all assigned programs Work as part of a collaborative, cross-functional team with members from other disciplines Provide statistical input into clinical development plans, clinical study protocols, clinical study reports
Später ansehen06.06.24 | Vollzeit | Kaiserslautern | BioNTech SEAccountable for all statistical aspects Work as part of a collaborative, cross-functional team with members from other disciplines Provide statistical input into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents, and publications ensuring accurate
Später ansehen06.06.24 | Vollzeit | Kaiserslautern | BioNTech SEFor all statistical aspects Serve as the biostatistics lead core team member for all assigned programs Work as part of a collaborative, cross-functional team with members from other disciplines Provide statistical input into clinical development plans, clinical study protocols, clinical study reports
Später ansehen06.06.24 | Vollzeit | Kaiserslautern | BioNTech SEFor all statistical aspects Serve as the biostatistics lead core team member for all assigned programs Work as part of a collaborative, cross-functional team with members from other disciplines Provide statistical input into clinical development plans, clinical study protocols, clinical study reports
Später ansehen06.06.24 | Vollzeit | Kaiserslautern | BioNTech SEAccountable for all statistical aspects Work as part of a collaborative, cross-functional team with members from other disciplines Provide statistical input into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents, and publications ensuring accurate
Später ansehen06.06.24 | Vollzeit | Kaiserslautern | BioNTech SEAccountable for all statistical aspects Work as part of a collaborative, cross-functional team with members from other disciplines Provide statistical input into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents, and publications ensuring accurate
Später ansehen06.06.24 | Vollzeit | Kaiserslautern | BioNTech SEAccountable for all statistical aspects Work as part of a collaborative, cross-functional team with members from other disciplines Provide statistical input into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents, and publications ensuring accurate
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