ICON plc
Senior CRA (Sponsor dedicated)(m/w/x)
Vollzeitmit HomeofficeSenior
Frankfurt am Main
Neuer Job?Nejo!
Dein persönlicher KI-Karriere-Agent
ICICON plc
Clinical Research Associate(m/w/x)
Frankfurt am Main
Vollzeitmit HomeofficeSenior
Nejo KI-Zusammenfassung
Monitoring clinical trial sites for protocol adherence and GCP compliance. Extensive CRA experience and regulatory knowledge required. 6 weeks vacation, company car for private use.
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
- Proven ability to manage multiple projects
- Strong organizational skills
- Strong problem-solving skills
- Expertise in monitoring practices
- Expertise in data integrity
- Expertise in site management
- Proficiency in relevant clinical trial software
- Proficiency in relevant clinical trial tools
- Excellent communication skills
- Excellent interpersonal skills
- Excellent stakeholder management skills
- Ability to influence within a complex environment
- Ability to drive compliance within a complex environment
- Ability to travel at least 40-60% of the time
- Encouraged to apply even if not meeting all requirements
Aufgaben
- Monitor clinical trial sites for protocol adherence
- Ensure compliance with regulatory requirements
- Uphold Good Clinical Practice (GCP) standards
- Conduct site visits to assess performance
- Resolve site issues and provide support
- Ensure successful trial execution
- Collaborate with cross-functional teams
- Ensure timely data collection
- Ensure accurate data collection
- Ensure timely data reporting
- Ensure accurate data reporting
- Train site staff on trial conduct
- Guide site staff on trial conduct
- Train other CRAs on trial conduct
- Guide other CRAs on trial conduct
- Build relationships with site personnel
- Maintain relationships with site personnel
- Build relationships with stakeholders
- Maintain relationships with stakeholders
- Facilitate smooth trial operations
Berufserfahrung
- ca. 4 - 6 Jahre
Ausbildung
- Master-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- clinical trial software
- clinical trial tools
Benefits
Gesundheits- & Fitnessangebote
- Health insurance
- Health assessments
Betriebliche Altersvorsorge
- 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
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VollzeitRemoteBerufserfahrenFrankfurt am Main - ICON plc
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Vollzeitmit HomeofficeSeniorFrankfurt am Main - ICON plc
Clinical Research Associate II / Senior Clinical Research Associate Biotech(m/w/x)
Vollzeitmit HomeofficeSeniorFrankfurt am Main - ICON plc
(Senior) Clinical Research Associate - sponsor dedicated(m/w/x)
Vollzeitmit HomeofficeSeniorFrankfurt am Main
ICICON plc
Clinical Research Associate(m/w/x)
Frankfurt am Main
Vollzeitmit HomeofficeSenior
Nejo KI-Zusammenfassung
Monitoring clinical trial sites for protocol adherence and GCP compliance. Extensive CRA experience and regulatory knowledge required. 6 weeks vacation, company car for private use.
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
- Proven ability to manage multiple projects
- Strong organizational skills
- Strong problem-solving skills
- Expertise in monitoring practices
- Expertise in data integrity
- Expertise in site management
- Proficiency in relevant clinical trial software
- Proficiency in relevant clinical trial tools
- Excellent communication skills
- Excellent interpersonal skills
- Excellent stakeholder management skills
- Ability to influence within a complex environment
- Ability to drive compliance within a complex environment
- Ability to travel at least 40-60% of the time
- Encouraged to apply even if not meeting all requirements
Aufgaben
- Monitor clinical trial sites for protocol adherence
- Ensure compliance with regulatory requirements
- Uphold Good Clinical Practice (GCP) standards
- Conduct site visits to assess performance
- Resolve site issues and provide support
- Ensure successful trial execution
- Collaborate with cross-functional teams
- Ensure timely data collection
- Ensure accurate data collection
- Ensure timely data reporting
- Ensure accurate data reporting
- Train site staff on trial conduct
- Guide site staff on trial conduct
- Train other CRAs on trial conduct
- Guide other CRAs on trial conduct
- Build relationships with site personnel
- Maintain relationships with site personnel
- Build relationships with stakeholders
- Maintain relationships with stakeholders
- Facilitate smooth trial operations
Berufserfahrung
- ca. 4 - 6 Jahre
Ausbildung
- Master-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- clinical trial software
- clinical trial tools
Benefits
Gesundheits- & Fitnessangebote
- Health insurance
- Health assessments
Betriebliche Altersvorsorge
- 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
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Vollzeitmit HomeofficeSeniorFrankfurt am Main - ICON plc
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Senior CRA(m/w/x)
Vollzeitmit HomeofficeSeniorFrankfurt am Main - ICON plc
Clinical Research Associate II / Senior Clinical Research Associate Biotech(m/w/x)
Vollzeitmit HomeofficeSeniorFrankfurt am Main - ICON plc
(Senior) Clinical Research Associate - sponsor dedicated(m/w/x)
Vollzeitmit HomeofficeSeniorFrankfurt am Main