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Clinical Research Associate II / Senior Clinical Research Associate Biotech(m/w/x)
Monitoring clinical trial sites for biotech studies, ensuring protocol adherence and data integrity. Extensive clinical research monitoring experience and advanced life sciences degree required. Work on global biotech clinical trials.
Anforderungen
- Advanced degree in a relevant field such as life sciences, nursing, or medicine
- Extensive experience as a Clinical Research Associate
- Proven ability to manage multiple sites and projects
- Expertise in monitoring practices and data integrity
- Excellent communication skills in German and English
Aufgaben
- Monitor clinical trial sites for protocol adherence
- Conduct site visits to assess performance and resolve issues
- Collaborate with teams for accurate data collection and reporting
- Provide training and guidance to site staff and CRAs
- Build and maintain relationships with site personnel and stakeholders
Berufserfahrung
- ca. 4 - 6 Jahre
Ausbildung
- Master-Abschluss
Sprachen
- Deutsch – verhandlungssicher
- Englisch – verhandlungssicher
Tools & Technologien
- clinical trial software
Benefits
Mehr Urlaubstage
- Various annual leave entitlements
Gesundheits- & Fitnessangebote
- Health insurance offerings
Betriebliche Altersvorsorge
- Competitive retirement planning
Mentale Gesundheitsförderung
- Global Employee Assistance Programme
Sonstige Vorteile
- Life assurance
- Flexible optional benefits
Noch nicht perfekt?
- ICON plcVollzeitmit HomeofficeSeniorFrankfurt am Main
- 176 ICON Clinical Research Germany GmbH
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Clinical Research Associate II / Senior Clinical Research Associate Biotech(m/w/x)
Monitoring clinical trial sites for biotech studies, ensuring protocol adherence and data integrity. Extensive clinical research monitoring experience and advanced life sciences degree required. Work on global biotech clinical trials.
Anforderungen
- Advanced degree in a relevant field such as life sciences, nursing, or medicine
- Extensive experience as a Clinical Research Associate
- Proven ability to manage multiple sites and projects
- Expertise in monitoring practices and data integrity
- Excellent communication skills in German and English
Aufgaben
- Monitor clinical trial sites for protocol adherence
- Conduct site visits to assess performance and resolve issues
- Collaborate with teams for accurate data collection and reporting
- Provide training and guidance to site staff and CRAs
- Build and maintain relationships with site personnel and stakeholders
Berufserfahrung
- ca. 4 - 6 Jahre
Ausbildung
- Master-Abschluss
Sprachen
- Deutsch – verhandlungssicher
- Englisch – verhandlungssicher
Tools & Technologien
- clinical trial software
Benefits
Mehr Urlaubstage
- Various annual leave entitlements
Gesundheits- & Fitnessangebote
- Health insurance offerings
Betriebliche Altersvorsorge
- Competitive retirement planning
Mentale Gesundheitsförderung
- Global Employee Assistance Programme
Sonstige Vorteile
- Life assurance
- Flexible optional benefits
Über das Unternehmen
ICON plc
Branche
Healthcare
Beschreibung
ICON plc is a world-leading healthcare intelligence and clinical research organization.
Noch nicht perfekt?
- ICON plc
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