ICON plc
Sr. Clinical Research Associate(m/w/x)
Vollzeitmit HomeofficeBerufserfahren
Wien
Neuer Job?Nejo!
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ICICON plc
Senior Clinical Research Associate(m/w/x)
Wien
Vollzeitmit HomeofficeSenior
Nejo KI-Zusammenfassung
Oversight of clinical study sites, ensuring protocol and regulatory compliance for a global CRO. Extensive clinical monitoring experience required. Frequent site visits, with global EAP and 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 simultaneously
- 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 and tools
- Excellent communication skills
- Excellent interpersonal skills
- Excellent stakeholder management skills
- Ability to influence and drive compliance in complex environment
- Ability to travel at least 60% (international and domestic)
- Valid driver’s license
Aufgaben
- Monitor clinical trial sites for protocol, regulatory, and GCP adherence.
- Conduct site visits.
- Assess site performance.
- Resolve site-related issues.
- Provide support for successful trial execution.
- Collaborate with cross-functional teams for timely, accurate data collection.
- Collaborate with cross-functional teams for timely, accurate data reporting.
- Train and guide site staff and CRAs on trial conduct.
- 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
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 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?
- IQVIA
Clinical Research Associate II or Senior Clinical Research Associate I(m/w/x)
Vollzeitmit HomeofficeSeniorWienab 4.200 / Monat - IQVIA Biotech
Clinical Research Associate 2(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenWienab 4.000 / Monat - AOP Health
Clinical Site Management Lead(m/w/x)
Vollzeitmit HomeofficeSeniorWienab 45.080 / Jahr - IQVIA
Clinical Research Associate I or II(m/w/x)
Vollzeitmit HomeofficeJuniorWienab 3.600 / Monat
ICICON plc
Senior Clinical Research Associate(m/w/x)
Wien
Vollzeitmit HomeofficeSenior
Nejo KI-Zusammenfassung
Oversight of clinical study sites, ensuring protocol and regulatory compliance for a global CRO. Extensive clinical monitoring experience required. Frequent site visits, with global EAP and 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 simultaneously
- 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 and tools
- Excellent communication skills
- Excellent interpersonal skills
- Excellent stakeholder management skills
- Ability to influence and drive compliance in complex environment
- Ability to travel at least 60% (international and domestic)
- Valid driver’s license
Aufgaben
- Monitor clinical trial sites for protocol, regulatory, and GCP adherence.
- Conduct site visits.
- Assess site performance.
- Resolve site-related issues.
- Provide support for successful trial execution.
- Collaborate with cross-functional teams for timely, accurate data collection.
- Collaborate with cross-functional teams for timely, accurate data reporting.
- Train and guide site staff and CRAs on trial conduct.
- 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
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 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
Sr. Clinical Research Associate(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenWien - IQVIA
Clinical Research Associate II or Senior Clinical Research Associate I(m/w/x)
Vollzeitmit HomeofficeSeniorWienab 4.200 / Monat - IQVIA Biotech
Clinical Research Associate 2(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenWienab 4.000 / Monat - AOP Health
Clinical Site Management Lead(m/w/x)
Vollzeitmit HomeofficeSeniorWienab 45.080 / Jahr - IQVIA
Clinical Research Associate I or II(m/w/x)
Vollzeitmit HomeofficeJuniorWienab 3.600 / Monat