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

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

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

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

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

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

, 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