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

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

apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity

efforts by providing regional insights relevant to clinical trial design, evidence generation, and reimbursement pathways • University degree in Health Economics, Public Health, Life Sciences, Pharmacy, Economics, or a

systems, aiming to enhance treatment outcomes and patient satisfaction. • Partner with HCPs to refine patient pathways and treatment protocols in accordance with current clinical guidelines and industry best practices, thereby

-related clinical and scientific literature to position both yourself and the team as trusted subject matter experts. • Strategically plan and engage with national Key External Experts (KEEs) to maximize scientific exchange and