23.05.24 | Vollzeit | Essen | 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 ansehen23.05.24 | Vollzeit | Neu-Isenburg | GBG Forschungs GmbHRelevant experience in the conduct of pharmaceutical trials in oncology You have experience with scientific work and clinical trials including work according to Good Clinical Practice (GCP) You enjoy working independently in highly motivated and dynamic team You have the following skills strong
Später ansehen23.05.24 | Vollzeit | Neu-Isenburg | GBG Forschungs GmbHRelevant experience in the conduct of pharmaceutical trials in oncology You have experience with scientific work and clinical trials including work according to Good Clinical Practice (GCP) You enjoy working independently in highly motivated and dynamic team You have the following skills strong
Später ansehen16.05.24 | Vollzeit | Neu-Isenburg | GBG Forschungs GmbHmanagement - You are tech savvy and confident in using MS Office applications, as well as MS Teams and reference management software (e.g. EndNote) - You have a very good command of written and spoken German and English - Participation in exciting clinical trials and translational research projects
Später ansehen11.05.24 | Vollzeit | Marburg | Nexelis Marburg GmbHYou will be part of the Technical Lab Support Team mainly on-site focused on a comprehensive clinical trial management in the variety of indications. In this team you will be mainly involved in operational and organizational qualification/validation and life-cycle management of laboratory
Später ansehen24.05.24 | Vollzeit | Kaiserslautern | BioNTech SEMRNA clinical trial projects. As part of our Operational QA Team, you will be based in Mainz at our IMP manufacturing site. This exiting role will bring you in contact not only with GMP related questions, but also with questions connected to other quality management systems (ISO 9001, ISO 13485 etc
Später ansehen24.05.24 | Vollzeit | Kaiserslautern | BioNTech SEMRNA clinical trial projects. As part of our Operational QA Team, you will be based in Mainz at our IMP manufacturing site. This exiting role will bring you in contact not only with GMP related questions, but also with questions connected to other quality management systems (ISO 9001, ISO 13485 etc
Später ansehen24.05.24 | Vollzeit | Kaiserslautern | BioNTech SEMRNA clinical trial projects. As part of our Operational QA Team, you will be based in Mainz at our IMP manufacturing site. This exiting role will bring you in contact not only with GMP related questions, but also with questions connected to other quality management systems (ISO 9001, ISO 13485 etc
Später ansehen24.05.24 | Vollzeit | Kaiserslautern | BioNTech SEMRNA clinical trial projects. As part of our Operational QA Team, you will be based in Mainz at our IMP manufacturing site. This exiting role will bring you in contact not only with GMP related questions, but also with questions connected to other quality management systems (ISO 9001, ISO 13485 etc
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