01.06.24 | Vollzeit | Jena | ZEISSOf applications for approval of clinical studies to authorities and ethics committees. - Organization and execution of clinical studies with coordination of all parties involved for planning and meeting timelines, milestones and budgets, reporting on project progress, preparing presentations to management
Später ansehen31.05.24 | Vollzeit | Jena | ZEISSIt takes less than 10 minutes. - Participate in complex project product development with R&D and PM, identify potential clinically relevant issues emerging from (absence of) features and their clinical consequences, define and implement the appropriate clinical evaluation strategy and necessary clinical
Später ansehen31.05.24 | Vollzeit | München | ZEISSIt takes less than 10 minutes. - Participate in project product development with R&D and PM, identify potential clinically relevant issues emerging from (absence of) features and their clinical consequences, define and implement the appropriate clinical evaluation strategy and necessary clinical studies
Später ansehen31.05.24 | Vollzeit | Pullach im Isartal | WuXi AppTecResources to all projects and activities. And make adjustments whenever is needed, ensuring that every project meets timeline and Quality requirements. When significant quality impact of a project is identified, immediately report to upper management and communicate with the customers (including proposal
Später ansehen31.05.24 | Vollzeit | Straßlach-Dingharting | WuXi AppTecResources to all projects and activities. And make adjustments whenever is needed, ensuring that every project meets timeline and Quality requirements. When significant quality impact of a project is identified, immediately report to upper management and communicate with the customers (including proposal
Später ansehen31.05.24 | Vollzeit | Oberhaching | WuXi AppTecResources to all projects and activities. And make adjustments whenever is needed, ensuring that every project meets timeline and Quality requirements. When significant quality impact of a project is identified, immediately report to upper management and communicate with the customers (including proposal
Später ansehen21.05.24 | Vollzeit | München | Daiichi Sankyo Europe GmbHAssuming 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 of the drug. Specific responsibilities
Später ansehen23.05.24 | Vollzeit | München | Otsuka Novel Products GmbHOf the project, from medical research and clinical development, to commercialization, pharmacovigilance, regulatory issues, access strategies, strategic alliances and more. For our Medical Affairs Team based in Munich, Germany, with remote working options, we are recruiting one (Senior) Manager Medical Affairs
Später ansehen22.05.24 | Vollzeit | Garching bei München | ITM Isotope Technologies Munich SEAnd 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 internally (e.g. Quality Assurance) as well as externally
Später ansehenVerpassen Sie nie wieder einen passenden Job!
Alle Jobs für Clinical Project Manager in München Landkreis kostenlos abonnieren.