ICON plc
Senior CRA (Sponsor Dedicated)(m/w/x)
Vollzeitmit HomeofficeSenior
Frankfurt am Main
Neuer Job?Nejo!
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ICICON plc
Senior CRA (Sponsor dedicated)(m/w/x)
Frankfurt am Main
Vollzeitmit HomeofficeSenior
Nejo KI-Zusammenfassung
On-site monitoring of clinical trial sites for a dedicated sponsor's drug development. Advanced degree in life sciences and extensive clinical trial monitoring experience required. Focus on a single sponsor's clinical trial portfolio.
Anforderungen
- Advanced degree in life sciences, nursing, or medicine
- Extensive experience as Clinical Research Associate
- Understanding of clinical trial processes and regulations
- Ability to manage multiple sites and projects
- Strong organizational and problem-solving skills
- Expertise in monitoring practices and data integrity
- Proficiency in clinical trial software and tools
- Excellent communication and stakeholder management skills
- Ability to influence and drive compliance
- Ability to travel 60% of the time
- Possession of a valid driver’s license
Aufgaben
- Monitor clinical trial sites for protocol adherence
- Ensure compliance with regulatory and GCP standards
- Conduct site visits to assess performance
- Resolve site issues to ensure trial execution
- Collaborate with cross-functional teams for data reporting
- Train and guide site staff and colleagues
- Maintain high standards of clinical trial conduct
- Build effective relationships with site personnel
Ausbildung
- Master-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- clinical trial software
Benefits
Attraktive Vergütung
- Competitive salary
Gesundheits- & Fitnessangebote
- Health insurance offerings
- Health assessments
Betriebliche Altersvorsorge
- Competitive retirement planning
Mentale Gesundheitsförderung
- Global Employee Assistance Programme
Sonstige Vorteile
- Life assurance
Kinderbetreuung
- Childcare vouchers
Firmenfahrrad
- Bike purchase schemes
Mitarbeiterrabatte
- Discounted gym memberships
Öffi Tickets
- Subsidised travel passes
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens ICON plc erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.
Noch nicht perfekt?
- ICON plc
(Senior) Clinical Research Associate - sponsor dedicated(m/w/x)
Vollzeitmit HomeofficeSeniorFrankfurt am Main - ICON plc
Clinical Research Associate - Sponsor Dedicated(m/w/x)
VollzeitRemoteBerufserfahrenFrankfurt am Main - ICON plc
Senior CRA(m/w/x)
Vollzeitmit HomeofficeSeniorFrankfurt am Main - 176 ICON Clinical Research Germany GmbH
Senior Clinical Research Associate (SCRA) - sponsor dedicated(m/w/x)
VollzeitRemoteSeniorFrankfurt am Main
ICICON plc
Senior CRA (Sponsor dedicated)(m/w/x)
Frankfurt am Main
Vollzeitmit HomeofficeSenior
Nejo KI-Zusammenfassung
On-site monitoring of clinical trial sites for a dedicated sponsor's drug development. Advanced degree in life sciences and extensive clinical trial monitoring experience required. Focus on a single sponsor's clinical trial portfolio.
Anforderungen
- Advanced degree in life sciences, nursing, or medicine
- Extensive experience as Clinical Research Associate
- Understanding of clinical trial processes and regulations
- Ability to manage multiple sites and projects
- Strong organizational and problem-solving skills
- Expertise in monitoring practices and data integrity
- Proficiency in clinical trial software and tools
- Excellent communication and stakeholder management skills
- Ability to influence and drive compliance
- Ability to travel 60% of the time
- Possession of a valid driver’s license
Aufgaben
- Monitor clinical trial sites for protocol adherence
- Ensure compliance with regulatory and GCP standards
- Conduct site visits to assess performance
- Resolve site issues to ensure trial execution
- Collaborate with cross-functional teams for data reporting
- Train and guide site staff and colleagues
- Maintain high standards of clinical trial conduct
- Build effective relationships with site personnel
Ausbildung
- Master-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- clinical trial software
Benefits
Attraktive Vergütung
- Competitive salary
Gesundheits- & Fitnessangebote
- Health insurance offerings
- Health assessments
Betriebliche Altersvorsorge
- Competitive retirement planning
Mentale Gesundheitsförderung
- Global Employee Assistance Programme
Sonstige Vorteile
- Life assurance
Kinderbetreuung
- Childcare vouchers
Firmenfahrrad
- Bike purchase schemes
Mitarbeiterrabatte
- Discounted gym memberships
Öffi Tickets
- Subsidised travel passes
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens ICON plc erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.
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
Senior CRA (Sponsor Dedicated)(m/w/x)
Vollzeitmit HomeofficeSeniorFrankfurt am Main - ICON plc
(Senior) Clinical Research Associate - sponsor dedicated(m/w/x)
Vollzeitmit HomeofficeSeniorFrankfurt am Main - ICON plc
Clinical Research Associate - Sponsor Dedicated(m/w/x)
VollzeitRemoteBerufserfahrenFrankfurt am Main - ICON plc
Senior CRA(m/w/x)
Vollzeitmit HomeofficeSeniorFrankfurt am Main - 176 ICON Clinical Research Germany GmbH
Senior Clinical Research Associate (SCRA) - sponsor dedicated(m/w/x)
VollzeitRemoteSeniorFrankfurt am Main