31.05.24 | Vollzeit | Neu-Isenburg | GBG Forschungs GmbHMedical Advisor (m/w/d) Deine wesentlichen Aufgaben • Betreuung von klinischen Studien mit Verantwortlichkeit für die medizinischen Inhalte und die Sicherheit der Patienten inkl. Medical Monitoring, Pharmakovigilanz und Bewertung von Referenzendokumenten • Medizinische Beratung von externen
Später ansehen10.06.24 | Vollzeit | JobLeads GmbH | 100.000 € - 125.000 € Organizational changes with the aim to support the achievement of business and personal goals. This role will act as a key enabler to inspire and drive change. This position will report directly to the VP, HR of EME with functional reporting line to VP, ClinicalOps, CEC Cluster. This position will be based
Später ansehen29.05.24 | Vollzeit | Galimedix GmbHclinical study documents, including study protocols, patient information, IB, study plans and manuals, and reports. - Execute of clinical trials. Delivery of project activities, full range of monitoring activities from start-up to close-out of a clinical trial. - Develop Protocol Deviation Plans
Später ansehen29.05.24 | Vollzeit | Böblingen | Philips GmbHAnd communication protocols for our patient monitoring products which enables connectivity and interoperability with other clinical devices of other vendors. The Service-oriented Device Connectivity Standard 11073 is the basis for your activities. With medical devices interoperating with each other in a clinical
Später ansehen11.06.24 | Vollzeit | Frankfurt am Main, Poznań, Wie | BioNTech SERequirements for trial-specific intended purposes of tests in our clinical programs. Monitoring of development activities and development plans of external diagnostic partners and alignment with BNT's clinical timelines Review partnership contracts to identify critical development and regulatory submission
Später ansehen11.06.24 | Vollzeit | Hanau, Darmstadt, Offenbach am | BioNTech SERequirements for trial-specific intended purposes of tests in our clinical programs. Monitoring of development activities and development plans of external diagnostic partners and alignment with BNT's clinical timelines Review partnership contracts to identify critical development and regulatory submission
Später ansehen11.06.24 | Vollzeit | Wiesbaden, Frankfurt am Main | BioNTech SERequirements for trial-specific intended purposes of tests in our clinical programs. Monitoring of development activities and development plans of external diagnostic partners and alignment with BNT's clinical timelines Review partnership contracts to identify critical development and regulatory submission
Später ansehen11.06.24 | Vollzeit | Ludwigshafen am Rhein, Mannhei | BioNTech SERequirements for trial-specific intended purposes of tests in our clinical programs. Monitoring of development activities and development plans of external diagnostic partners and alignment with BNT's clinical timelines Review partnership contracts to identify critical development and regulatory submission
Später ansehen11.06.24 | Vollzeit | Mainz, Worms, Ludwigshafen am | BioNTech SERequirements for trial-specific intended purposes of tests in our clinical programs. Monitoring of development activities and development plans of external diagnostic partners and alignment with BNT's clinical timelines Review partnership contracts to identify critical development and regulatory submission
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