ICON plc
Clinical Research Associate II / Senior CRA(m/w/x)
Vollzeitmit HomeofficeSenior
Mannheim
Neuer Job?Nejo!
Dein persönlicher KI-Karriere-Agent
ICICON plc
Clinical Research Coordinator II (Site Management Associate II)(m/w/x)
Mannheim, Frankfurt am Main
Vollzeitmit HomeofficeBerufserfahren
Nejo KI-Zusammenfassung
Coordinating monitoring activities and resolving site issues for clinical trials. Bachelor's degree and clinical research experience required. 4 weeks vacation, health insurance.
Anforderungen
- Bachelor’s degree in life sciences, healthcare administration, or clinical research
- Experience in clinical research, site management, or monitoring
- Solid understanding of clinical trial processes and GCP guidelines
- Strong organizational and project management skills
- Ability to handle multiple priorities and deadlines
- Excellent analytical skills and attention to detail
- Focus on maintaining high-quality standards
- Exceptional communication and interpersonal skills
- Ability to build and maintain effective relationships with site personnel and cross-functional teams
- Fluent German
- Ability to go to office in Munich
- Interest in the role
- Encouraged to apply even if not meeting all requirements
Aufgaben
- Coordinate monitoring activities at clinical trial sites
- Ensure adherence to study protocols
- Resolve site-related issues promptly
- Assist in preparing regulatory documents
- Review regulatory documents
- Ensure site activities comply with GCP
- Ensure site activities comply with applicable regulations
- Collaborate with cross-functional teams
- Facilitate effective communication with trial sites
- Provide support to trial sites
- Track site performance metrics
- Analyze site performance data
- Provide reports on site management efficiency
- Participate in training initiatives
- Mentor junior staff
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Deutsch – fließend
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
- Flexible country-specific optional benefits
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 Clinical Research Germany GmbH
Clinical Trial Assistant (CTA)(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenMannheim - 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
ICICON plc
Clinical Research Coordinator II (Site Management Associate II)(m/w/x)
Mannheim, Frankfurt am Main
Vollzeitmit HomeofficeBerufserfahren
Nejo KI-Zusammenfassung
Coordinating monitoring activities and resolving site issues for clinical trials. Bachelor's degree and clinical research experience required. 4 weeks vacation, health insurance.
Anforderungen
- Bachelor’s degree in life sciences, healthcare administration, or clinical research
- Experience in clinical research, site management, or monitoring
- Solid understanding of clinical trial processes and GCP guidelines
- Strong organizational and project management skills
- Ability to handle multiple priorities and deadlines
- Excellent analytical skills and attention to detail
- Focus on maintaining high-quality standards
- Exceptional communication and interpersonal skills
- Ability to build and maintain effective relationships with site personnel and cross-functional teams
- Fluent German
- Ability to go to office in Munich
- Interest in the role
- Encouraged to apply even if not meeting all requirements
Aufgaben
- Coordinate monitoring activities at clinical trial sites
- Ensure adherence to study protocols
- Resolve site-related issues promptly
- Assist in preparing regulatory documents
- Review regulatory documents
- Ensure site activities comply with GCP
- Ensure site activities comply with applicable regulations
- Collaborate with cross-functional teams
- Facilitate effective communication with trial sites
- Provide support to trial sites
- Track site performance metrics
- Analyze site performance data
- Provide reports on site management efficiency
- Participate in training initiatives
- Mentor junior staff
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Deutsch – fließend
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
- Flexible country-specific optional benefits
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 CRA(m/w/x)
Vollzeitmit HomeofficeSeniorMannheim - ICON Clinical Research Germany GmbH
Clinical Trial Assistant (CTA)(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenMannheim - 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