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Senior Clinical Research Associate(m/w/x)
Monitoring clinical trial sites for protocol adherence and data integrity within a global healthcare intelligence firm. Extensive CRA experience and an advanced life sciences degree required. International site visits, managing multiple clinical projects.
Anforderungen
- Advanced degree in 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 and interpersonal skills
- Ability to travel at least 60% of the time
- Fluency 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
Benefits
Mehr Urlaubstage
- Various annual leave entitlements
Gesundheits- & Fitnessangebote
- Health insurance offerings
Betriebliche Altersvorsorge
- Retirement planning offerings
Mentale Gesundheitsförderung
- Global Employee Assistance Programme
Sonstige Vorteile
- Life assurance
- Flexible optional benefits
Noch nicht perfekt?
- 176 ICON Clinical Research Germany GmbHVollzeitRemoteSeniorFrankfurt am Main
- ICON plc
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Senior Clinical Research Associate(m/w/x)
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Senior Clinical Research Associate(m/w/x)
Monitoring clinical trial sites for protocol adherence and data integrity within a global healthcare intelligence firm. Extensive CRA experience and an advanced life sciences degree required. International site visits, managing multiple clinical projects.
Anforderungen
- Advanced degree in 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 and interpersonal skills
- Ability to travel at least 60% of the time
- Fluency 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
Benefits
Mehr Urlaubstage
- Various annual leave entitlements
Gesundheits- & Fitnessangebote
- Health insurance offerings
Betriebliche Altersvorsorge
- Retirement planning offerings
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?
- 176 ICON Clinical Research Germany GmbH
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