Senior Clinical Research Associate – Germany Chloe O’Shea is pleased to be working with a small global CRO recognised for driving innovation and excellence in clinical development. We are seeking an experienced Clinical

von einer Zusatzausbildung zur Studienassistenz, Clinical Research Associate (CRA) oder zur Klinischen Monitorin / zum Klinischen Monitor.Sie verfügen über gute Englischkenntnisse in Wort und Schrift30 Tage Urlaub, 40 Stunden / Woche

von einer Zusatzausbildung zur Studienassistenz, Clinical Research Associate (CRA) oder zur Klinischen Monitorin / zum Klinischen Monitor.Sie verfügen über gute Englischkenntnisse in Wort und Schrift30 Tage Urlaub, 40 Stunden / Woche

von einer Zusatzausbildung zur Studienassistenz, Clinical Research Associate (CRA) oder zur Klinischen Monitorin / zum Klinischen Monitor.Sie verfügen über gute Englischkenntnisse in Wort und Schrift30 Tage Urlaub, 40 Stunden / Woche

von einer Zusatzausbildung zur Studienassistenz, Clinical Research Associate (CRA) oder zur Klinischen Monitorin / zum Klinischen Monitor.Sie verfügen über gute Englischkenntnisse in Wort und Schrift30 Tage Urlaub, 40 Stunden / Woche

Our client, a leading player in the clinical research market, is currently seeking CRA's and CRA II to support long term sponsors across Germany. As a CRA/CRA II, you will have the opportunity to work on challenging

Our client, a leading player in the clinical research market, is currently seeking CRA's and CRA II to support long term sponsors across Germany. As a CRA/CRA II, you will have the opportunity to work on challenging

Our client, a leading player in the clinical research market, is currently seeking CRA's and CRA II to support long term sponsors across Germany. As a CRA/CRA II, you will have the opportunity to work on challenging

Sie Vorkenntnisse in der Studienorganisation, z.B. in Form von einer Zusatzausbildung zur Studienassistenz, Clinical Research Associate (CRA) oder zur Klinischen Monitorin / zum Klinischen Monitor.Sie haben Kenntnisse in ICH/GCP.Sie

. • Kandidatengewinnung im regulierten Umfeld: Du findest hochqualifizierte Talente in einem engen Kandidatenmarkt - ob Regulatory Affairs Experte, GMP-Consultant oder Clinical Research Associate - und präsentierst sie professionell

Sie Vorkenntnisse in der Studienorganisation, z.B. in Form von einer Zusatzausbildung zur Studienassistenz, Clinical Research Associate (CRA) oder zur Klinischen Monitorin / zum Klinischen Monitor.Sie haben Kenntnisse in ICH/GCP.Sie

ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly

ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly

ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly

ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly

ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly

ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly