mit internationalen Studiengruppen ist die AGO eine der stärksten Studiengruppen in der gynäkologischen Onkologie weltweit. Wir suchen für unsere Studiensekretariate in Wiesbaden und Essen Clinical Trial Manager / Studienkoordinatoren

Time for change – time for a new job! You are a clinical trial Administrator and looking for a new professional challenge in a pharmaceutical company? Then stop searching! We offer the job you are looking for: Our

Time for change – time for a new job! You are a clinical trial Administrator and looking for a new professional challenge in a pharmaceutical company? Then stop searching! We offer the job you are looking for: Our

Time for change – time for a new job! You are a clinical trial Administrator and looking for a new professional challenge in a pharmaceutical company? Then stop searching! We offer the job you are looking for: Our

Time for change – time for a new job! You are a clinical trial Administrator and looking for a new professional challenge in a pharmaceutical company? Then stop searching! We offer the job you are looking for: Our

. • Responsible for global Supply Chain activities for Investigational Medicinal Products (IMPs) of national and international Phase I-IV clinical trials in the Therapeutic Area General Medicine • Function as the main point of contact

Time for change – time for a new job! You are a clinical trial Administrator and looking for a new professional challenge in a pharmaceutical company? Then stop searching! We offer the job you are looking for: Our

submissions for Clinical Trials with IMPs via CTIS)If applicable also work partly as CRA including • Monitor and manage clinical trials (phases I-IV) in compliance with protocol, ICH-GCP/ISO 14155, SOPs, and regulations. Serve as

submissions for Clinical Trials with IMPs via CTIS)If applicable also work partly as CRA including • Monitor and manage clinical trials (phases I-IV) in compliance with protocol, ICH-GCP/ISO 14155, SOPs, and regulations. Serve as

submissions for Clinical Trials with IMPs via CTIS)If applicable also work partly as CRA including • Monitor and manage clinical trials (phases I-IV) in compliance with protocol, ICH-GCP/ISO 14155, SOPs, and regulations. Serve as

Trials with IMPs via CTIS). If applicable also work partly as CRA including: Monitor and manage clinical trials (phases I-IV) in compliance with protocol, ICH-GCP/ISO 14155, SOPs, and regulations. Serve as main point of contact

und internationalen Kongressen teil. • Du bist die Schnittstelle zwischen verschiedenen Fachabteilungen wie Clinical Trials, Produktmanagement, und Außendienst und schulst wissenschaftliche Inhalte nach innen und außen. • Du hast

zum nächstmöglichen Zeitpunkt eine*n Clinical Data Manager (w/m/d) – in Vollzeit – • In Ihrer Rolle als Clinical Data Manager stellen Sie die korrekte, vollständige und regelkonforme Erhebung sowie Aufbereitung der Studiendaten

collaboration, and accelerated intelligence.Learn about the Danaher Business System which makes everything possible.The Product Marketing Manager CC/IA is responsible for lifecycle management, marketing, and support of Clinical

collaboration, and accelerated intelligence.Learn about the Danaher Business System which makes everything possible.The Product Marketing Manager CC/IA is responsible for lifecycle management, marketing, and support of Clinical

collaboration, and accelerated intelligence.Learn about the Danaher Business System which makes everything possible.The Product Marketing Manager CC/IA is responsible for lifecycle management, marketing, and support of Clinical

collaboration, and accelerated intelligence.Learn about the Danaher Business System which makes everything possible.The Product Marketing Manager CC/IA is responsible for lifecycle management, marketing, and support of Clinical

collaboration, and accelerated intelligence.Learn about the Danaher Business System which makes everything possible.The Product Marketing Manager CC/IA is responsible for lifecycle management, marketing, and support of Clinical

upselling in key strategic accounts working in conjunction with Business Managers • Develop and continuously improve training curriculum, training materials and training tools, based on clinical trial experience, EW guidelines

, based on clinical trial experience, guidelines and SOPs • Responsible for certification of the centers, physicians and other related staff, as well as Edwards personnel and as outlined within Edwards' SOPs • Observe