176 ICON Clinical Research Germany GmbH
Senior Clinical Research Associate(m/w/x)
Vollzeitmit HomeofficeSenior
Mannheim
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ICICON plc
Clinical Research Associate II / Senior CRA(m/w/x)
Mannheim
Vollzeitmit HomeofficeSenior
Nejo KI-Zusammenfassung
Monitoring clinical trial sites for protocol and regulatory adherence, conducting site visits for a global CRO. Advanced life sciences degree and extensive clinical research monitoring experience required. Global travel, 24-hour professional support.
Anforderungen
- Advanced degree in life sciences, nursing, or medicine
- Extensive Clinical Research Associate experience
- Strong understanding of clinical trial processes
- Strong understanding of regulatory requirements
- Proven ability to manage multiple sites and projects
- Strong organizational skills
- Strong problem-solving skills
- Expertise in monitoring practices
- Expertise in data integrity
- Expertise in site management
- Proficiency in clinical trial software and tools
- Excellent communication skills
- Excellent interpersonal skills
- Excellent stakeholder management skills
- Ability to influence and drive compliance
- Ability to travel at least 60% (international/domestic)
- Valid driver’s license
Aufgaben
- Monitor clinical trial sites for protocol, regulatory, and GCP adherence
- Conduct site visits
- Assess site performance
- Resolve site issues
- Provide site support
- Collaborate with cross-functional teams for timely and accurate data collection and reporting
- Provide training and guidance to site staff and CRAs
- Build and maintain effective relationships with site personnel and stakeholders
Berufserfahrung
- ca. 4 - 6 Jahre
Ausbildung
- Master-Abschluss
Sprachen
- Englisch – verhandlungssicher
Benefits
Mehr Urlaubstage
- Various annual leave
Gesundheits- & Fitnessangebote
- Health insurance offerings
- Health assessments
Betriebliche Altersvorsorge
- Competitive retirement planning
Mentale Gesundheitsförderung
- Global Employee Assistance Programme
Sonstige Vorteile
- 24-hour professional support
- 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 Trial Manager(m/w/x)
VollzeitRemoteSeniorMannheim - 176 ICON Clinical Research Germany GmbH
Study Site Management Specialist(m/w/x)
Vollzeitmit HomeofficeSeniorMannheim - ICON plc
Study Start Up Associate(m/w/x)
Vollzeitmit HomeofficeJuniorMannheim - ICON Clinical Research Germany GmbH
Clinical Trial Assistant (CTA)(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenMannheim
ICICON plc
Clinical Research Associate II / Senior CRA(m/w/x)
Mannheim
Vollzeitmit HomeofficeSenior
Nejo KI-Zusammenfassung
Monitoring clinical trial sites for protocol and regulatory adherence, conducting site visits for a global CRO. Advanced life sciences degree and extensive clinical research monitoring experience required. Global travel, 24-hour professional support.
Anforderungen
- Advanced degree in life sciences, nursing, or medicine
- Extensive Clinical Research Associate experience
- Strong understanding of clinical trial processes
- Strong understanding of regulatory requirements
- Proven ability to manage multiple sites and projects
- Strong organizational skills
- Strong problem-solving skills
- Expertise in monitoring practices
- Expertise in data integrity
- Expertise in site management
- Proficiency in clinical trial software and tools
- Excellent communication skills
- Excellent interpersonal skills
- Excellent stakeholder management skills
- Ability to influence and drive compliance
- Ability to travel at least 60% (international/domestic)
- Valid driver’s license
Aufgaben
- Monitor clinical trial sites for protocol, regulatory, and GCP adherence
- Conduct site visits
- Assess site performance
- Resolve site issues
- Provide site support
- Collaborate with cross-functional teams for timely and accurate data collection and reporting
- Provide training and guidance to site staff and CRAs
- Build and maintain effective relationships with site personnel and stakeholders
Berufserfahrung
- ca. 4 - 6 Jahre
Ausbildung
- Master-Abschluss
Sprachen
- Englisch – verhandlungssicher
Benefits
Mehr Urlaubstage
- Various annual leave
Gesundheits- & Fitnessangebote
- Health insurance offerings
- Health assessments
Betriebliche Altersvorsorge
- Competitive retirement planning
Mentale Gesundheitsförderung
- Global Employee Assistance Programme
Sonstige Vorteile
- 24-hour professional support
- 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?
- 176 ICON Clinical Research Germany GmbH
Senior Clinical Research Associate(m/w/x)
Vollzeitmit HomeofficeSeniorMannheim - ICON plc
Senior Clinical Trial Manager(m/w/x)
VollzeitRemoteSeniorMannheim - 176 ICON Clinical Research Germany GmbH
Study Site Management Specialist(m/w/x)
Vollzeitmit HomeofficeSeniorMannheim - ICON plc
Study Start Up Associate(m/w/x)
Vollzeitmit HomeofficeJuniorMannheim - ICON Clinical Research Germany GmbH
Clinical Trial Assistant (CTA)(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenMannheim