23.05.24 | Vollzeit | München | Daiichi Sankyo Europe GmbHAnd 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 - Accountable for all aspects of safety
Später ansehen23.05.24 | Teilzeit, Vollzeit | Ludwigshafen am Rhein | AbbVie Deutschland GmbH & Co. KGSafety, and global medical affairs. The Manager works independently in partnership with experts in multiple disciplines to advance medicines to our patients. This means - Statistical planning, design, analysis, and reporting related to clinical studies and other scientific research studies, including
Später ansehen23.05.24 | Vollzeit | Neu-Isenburg | GBG Forschungs GmbHCommunication skills, analytical working and thinking skills, as well as a very good organizational and time management You are tech savvy and confident in using MS Office applications, as well as MS Teams and reference management software (e.g. EndNote) You have a very good command of written and spoken German
Später ansehen23.05.24 | Vollzeit | Neu-Isenburg | GBG Forschungs GmbHCommunication skills, analytical working and thinking skills, as well as a very good organizational and time management You are tech savvy and confident in using MS Office applications, as well as MS Teams and reference management software (e.g. EndNote) You have a very good command of written and spoken German
Später ansehen22.05.24 | Vollzeit | Garching bei München | ITM Isotope Technologies Munich SER&D Quality Manager (f/m/d) Your role Creation and maintenance of SOPs, documents and reports in Veeva Project Management and communication to internal and external partners Co-design of the QbD process Organization and documentation of laboratory equipment qualifications with project partners
Später ansehen22.05.24 | Vollzeit | Garching bei München | ITM Isotope Technologies Munich SER&D Quality Manager (f/m/d) Your role Creation and maintenance of SOPs, documents and reports in Veeva Project Management and communication to internal and external partners Co-design of the QbD process Organization and documentation of laboratory equipment qualifications with project partners
Später ansehen22.05.24 | Vollzeit | Garching bei München | ITM Isotope Technologies Munich SER&D Quality Manager (f/m/d) Your role Creation and maintenance of SOPs, documents and reports in Veeva Project Management and communication to internal and external partners Co-design of the QbD process Organization and documentation of laboratory equipment qualifications with project partners
Später ansehen21.05.24 | Vollzeit | Fürstenfeldbruck, Dachau, Germ | Daiichi Sankyo Europe GmbHFunctions and sites. The individual assuming this role may function as a key member of the Global Product Team in collaboration with Clinical Development, Regulatory, Project Management, Biostatistics, Pharmacology, and other departments to strategically manage benefit-risk throughout the lifecycle
Später ansehen21.05.24 | Vollzeit | Germering, Fürstenfeldbruck, D | Daiichi Sankyo Europe GmbHFunctions and sites. The individual assuming this role may function as a key member of the Global Product Team in collaboration with Clinical Development, Regulatory, Project Management, Biostatistics, Pharmacology, and other departments to strategically manage benefit-risk throughout the lifecycle
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