ICON plc
Clinical Research Associate(m/w/x)
Vollzeitmit HomeofficeSenior
Frankfurt am Main
Neuer Job?Nejo!
Dein persönlicher KI-Karriere-Agent
ICICON Clinical Research Germany GmbH
Freelance Snr CRA(m/w/x)
Frankfurt am Main
VollzeitFreelancemit HomeofficeSenior
Nejo KI-Zusammenfassung
Overseeing clinical trial activities and site visits for a global CRO. Extensive CRA experience and a scientific degree required. Annual leave entitlements, health insurance, and retirement planning.
Anforderungen
- Strong foundation in clinical trial monitoring
- Experience to work independently and guide others
- Bachelor's degree in scientific or healthcare field
- Extensive experience as Clinical Research Associate
- 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 complex environments
- Ability to drive compliance in complex environments
- Willingness to travel as required
Aufgaben
- Oversee clinical trial activities
- Manage trial adherence to protocols
- Ensure regulatory compliance
- Conduct site visits
- Assess site performance
- Resolve site issues
- Support site staff
- Collaborate with cross-functional teams
- Ensure timely data collection
- Maintain accurate data reporting
- Train site staff
- Guide other CRAs
- Build relationships with site personnel
- Maintain stakeholder relationships
- Facilitate smooth trial operations
Berufserfahrung
- ca. 4 - 6 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- clinical trial software
- clinical trial tools
Benefits
Mehr Urlaubstage
- Various annual leave entitlements
Gesundheits- & Fitnessangebote
- Health insurance offerings
- Health assessments
Betriebliche Altersvorsorge
- Retirement planning offerings
Mentale Gesundheitsförderung
- Global Employee Assistance Programme
Sonstige Vorteile
- Life assurance
Sonstige Zulagen
- 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 Clinical Research Germany GmbH 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.
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ICICON Clinical Research Germany GmbH
Freelance Snr CRA(m/w/x)
Frankfurt am Main
VollzeitFreelancemit HomeofficeSenior
Nejo KI-Zusammenfassung
Overseeing clinical trial activities and site visits for a global CRO. Extensive CRA experience and a scientific degree required. Annual leave entitlements, health insurance, and retirement planning.
Anforderungen
- Strong foundation in clinical trial monitoring
- Experience to work independently and guide others
- Bachelor's degree in scientific or healthcare field
- Extensive experience as Clinical Research Associate
- 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 complex environments
- Ability to drive compliance in complex environments
- Willingness to travel as required
Aufgaben
- Oversee clinical trial activities
- Manage trial adherence to protocols
- Ensure regulatory compliance
- Conduct site visits
- Assess site performance
- Resolve site issues
- Support site staff
- Collaborate with cross-functional teams
- Ensure timely data collection
- Maintain accurate data reporting
- Train site staff
- Guide other CRAs
- Build relationships with site personnel
- Maintain stakeholder relationships
- Facilitate smooth trial operations
Berufserfahrung
- ca. 4 - 6 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- clinical trial software
- clinical trial tools
Benefits
Mehr Urlaubstage
- Various annual leave entitlements
Gesundheits- & Fitnessangebote
- Health insurance offerings
- Health assessments
Betriebliche Altersvorsorge
- Retirement planning offerings
Mentale Gesundheitsförderung
- Global Employee Assistance Programme
Sonstige Vorteile
- Life assurance
Sonstige Zulagen
- 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 Clinical Research Germany GmbH 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.
Gefällt dir diese Stelle?
BetaDein Career Agent findet täglich ähnliche Jobs für dich.
Über das Unternehmen
ICON Clinical Research Germany GmbH
Branche
Healthcare
Beschreibung
ICON plc is a world-leading healthcare intelligence and clinical research organization focused on shaping the future of clinical development.
Noch nicht perfekt?
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