23.05.24 | Vollzeit | Wiesbaden | AGO Research GmbHStudiensekretariate in Wiesbaden und Essen Clinical Trial Manager - Studienkoordinatoren als Projektmanager (m/w/d) Beginn sofort/zum nächstmöglichen Zeitpunkt Dauer unbefristet in Vollzeit (40 h/Woche) Arbeitsort AGO Studiensekretariat Wiesbaden, AGO Studiensekretariat Essen - Mitarbeit bei der Betreuung
Später ansehen29.05.24 | Vollzeit | Wiesbaden | BioNTech SEOperational activities required to manage the lifecycle of biomarker samples in global Phase I-IV clinical trials Ensure biomarker sample related collection, tracking, and storage in compliance with the Clinical Trial Protocol and Patient Informed Consent Management of cross-functional integration
Später ansehen29.05.24 | Vollzeit | Wiesbaden | BioNTech SEOperational activities required to manage the lifecycle of biomarker samples in global Phase I-IV clinical trials Ensure biomarker sample related collection, tracking, and storage in compliance with the Clinical Trial Protocol and Patient Informed Consent Management of cross-functional integration
Später ansehen29.05.24 | Vollzeit | Wiesbaden | BioNTech SEOperational activities required to manage the lifecycle of biomarker samples in global Phase I-IV clinical trials Ensure biomarker sample related collection, tracking, and storage in compliance with the Clinical Trial Protocol and Patient Informed Consent Management of cross-functional integration
Später ansehen29.05.24 | Vollzeit | Wiesbaden | BioNTech SEOperational activities required to manage the lifecycle of biomarker samples in global Phase I-IV clinical trials Ensure biomarker sample related collection, tracking, and storage in compliance with the Clinical Trial Protocol and Patient Informed Consent Management of cross-functional integration
Später ansehen29.05.24 | Vollzeit | Wiesbaden | BioNTech SEOperational activities required to manage the lifecycle of biomarker samples in global Phase I-IV clinical trials Ensure biomarker sample related collection, tracking, and storage in compliance with the Clinical Trial Protocol and Patient Informed Consent Management of cross-functional integration
Später ansehen29.05.24 | Vollzeit | Wiesbaden | BioNTech SEOperational activities required to manage the lifecycle of biomarker samples in global Phase I-IV clinical trials Ensure biomarker sample related collection, tracking, and storage in compliance with the Clinical Trial Protocol and Patient Informed Consent Management of cross-functional integration
Später ansehen29.05.24 | Vollzeit | Wiesbaden | BioNTech SEOperational activities required to manage the lifecycle of biomarker samples in global Phase I-IV clinical trials Ensure biomarker sample related collection, tracking, and storage in compliance with the Clinical Trial Protocol and Patient Informed Consent Management of cross-functional integration
Später ansehen29.05.24 | Vollzeit | Wiesbaden | BioNTech SEOperational activities required to manage the lifecycle of biomarker samples in global Phase I-IV clinical trials Ensure biomarker sample related collection, tracking, and storage in compliance with the Clinical Trial Protocol and Patient Informed Consent Management of cross-functional integration
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