ICON plc
Clinical Research Associate II / Senior Clinical Research Associate Biotech(m/w/x)
Vollzeitmit HomeofficeSenior
Frankfurt am Main
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ICICON plc
Clinical Research Associate II / Senior Clinical Research Associate Large Pharma(m/w/x)
Frankfurt am Main
Vollzeitmit HomeofficeSenior
Nejo KI-Zusammenfassung
Monitoring clinical trial sites, ensuring protocol adherence and regulatory compliance for a global healthcare intelligence organization. Minimum 2 years Clinical Research Associate experience, with ICH-GCP knowledge, required. Extensive site travel, global trial exposure.
Anforderungen
- Master or Bachelor's degree in scientific or healthcare-related field
- Minimum 2 years experience as Clinical Research Associate
- Knowledge of clinical trial processes, regulations, and ICH-GCP
- Strong organizational, communication, and detail-oriented skills
- Ability to work independently and collaboratively
- Ability to manage multiple sites and projects
- Expertise in monitoring practices and data integrity
- Excellent communication skills in German and English
- Excellent interpersonal and stakeholder management skills
- Willingness to travel 60% and 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 teams for accurate data reporting
- Train site staff and junior CRAs
- Maintain relationships with site personnel and stakeholders
- Ensure data integrity and participant safety
Ausbildung
- Bachelor-AbschlussODER
- Master-Abschluss
Sprachen
- Deutsch – verhandlungssicher
- Englisch – verhandlungssicher
Tools & Technologien
- ICH-GCP guidelines
- clinical trial software
Benefits
Mehr Urlaubstage
- Various annual leave entitlements
Gesundheits- & Fitnessangebote
- Range of health insurance
- 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?
- 176 ICON Clinical Research Germany GmbH
CRA II/ Senior CRA(m/w/x)
Vollzeitmit HomeofficeSeniorFrankfurt am Main - ICON plc
(Senior) Clinical Research Associate - sponsor dedicated(m/w/x)
Vollzeitmit HomeofficeSeniorFrankfurt am Main - IQVIA
Clinical Research Associate 2 or Senior Clinical Research Associate 1(m/w/x)
Vollzeitmit HomeofficeSeniorFrankfurt am Main - ICON plc
Clinical Research Associate (CRA)(m/w/x)
VollzeitRemoteBerufserfahrenFrankfurt am Main
ICICON plc
Clinical Research Associate II / Senior Clinical Research Associate Large Pharma(m/w/x)
Frankfurt am Main
Vollzeitmit HomeofficeSenior
Nejo KI-Zusammenfassung
Monitoring clinical trial sites, ensuring protocol adherence and regulatory compliance for a global healthcare intelligence organization. Minimum 2 years Clinical Research Associate experience, with ICH-GCP knowledge, required. Extensive site travel, global trial exposure.
Anforderungen
- Master or Bachelor's degree in scientific or healthcare-related field
- Minimum 2 years experience as Clinical Research Associate
- Knowledge of clinical trial processes, regulations, and ICH-GCP
- Strong organizational, communication, and detail-oriented skills
- Ability to work independently and collaboratively
- Ability to manage multiple sites and projects
- Expertise in monitoring practices and data integrity
- Excellent communication skills in German and English
- Excellent interpersonal and stakeholder management skills
- Willingness to travel 60% and 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 teams for accurate data reporting
- Train site staff and junior CRAs
- Maintain relationships with site personnel and stakeholders
- Ensure data integrity and participant safety
Ausbildung
- Bachelor-AbschlussODER
- Master-Abschluss
Sprachen
- Deutsch – verhandlungssicher
- Englisch – verhandlungssicher
Tools & Technologien
- ICH-GCP guidelines
- clinical trial software
Benefits
Mehr Urlaubstage
- Various annual leave entitlements
Gesundheits- & Fitnessangebote
- Range of health insurance
- 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
Clinical Research Associate II / Senior Clinical Research Associate Biotech(m/w/x)
Vollzeitmit HomeofficeSeniorFrankfurt am Main - 176 ICON Clinical Research Germany GmbH
CRA II/ Senior CRA(m/w/x)
Vollzeitmit HomeofficeSeniorFrankfurt am Main - ICON plc
(Senior) Clinical Research Associate - sponsor dedicated(m/w/x)
Vollzeitmit HomeofficeSeniorFrankfurt am Main - IQVIA
Clinical Research Associate 2 or Senior Clinical Research Associate 1(m/w/x)
Vollzeitmit HomeofficeSeniorFrankfurt am Main - ICON plc
Clinical Research Associate (CRA)(m/w/x)
VollzeitRemoteBerufserfahrenFrankfurt am Main