IQVIA
Associate Manager or Manager, Clinical Operations(m/w/x)
VollzeitRemoteManagement
Frankfurt am Main
Neuer Job?Nejo!
Die KI-Suchmaschine für Jobs
ALAlimentiv
Clinical Operations Lead(m/w/x)
Frankfurt am Main
Vollzeitmit HomeofficeBerufserfahren
Nejo KI-Zusammenfassung
Overseeing clinical project compliance, training, and assessment visits for CRAs. Undergraduate degree and 7-9 years related experience required; Health Sciences, Life Sciences, or Nursing background preferred. Occasional site travel.
Anforderungen
- College diploma/degree
- 7-9 years related experience
- Undergraduate university degree (Bachelors or Honors Bachelors)
- 4-6 years' experience
- Health Sciences, Life Sciences or Nursing specialty preferred
- SoCRA and/or ACRP Certification/Designation
- Minimum of 3 years CRA experience
- Strong experience with EDC systems
- Proficiency with MS Office
- Strong written and verbal communication skills
- Highly effective interpersonal and organizational skills
- Proactivity
- Detail orientation
- Task-driven
- Highly organized
- Understanding of GCPs and local regulations
- Clinical monitoring knowledge
- Ability in report writing
- Strong understanding of clinical research documents
- Ability to handle multiple tasks
- Ability to meet deadlines in a dynamic environment
Aufgaben
- Oversee clinical operations for projects
- Ensure compliance with study protocols and regulations
- Act as a liaison between CRAs and the clinical project team
- Provide project-specific training for CRAs
- Conduct assessment visits with CRAs
- Implement enrollment and recruitment strategies
- Prepare monitoring plans and structural documentation
- Schedule monitoring visits and track performance metrics
- Manage issue escalation and corrective actions
- Develop study tools for site and CRA use
- Review visit reports for quality and compliance
- Track protocol deviations
- Support clinical operations objectives
- Monitor regional CRA compliance with study timelines
- Conduct co-monitoring visits as needed
- Assist in vendor management activities
- Proactively manage site and country performance
- Contribute to financial project management processes
- Manage investigator sites temporarily or permanently
- Conduct regular global CRA calls
- Attend meetings with Study Sponsor for status updates
- Provide operational support to the monitoring team
- Train and mentor regional CRAs on study procedures
- Serve as the first point of contact for CRAs
- Liaise with line managers for CRA assignments
- Conduct CRA assessment visits to evaluate performance
- Develop training materials and study tools
- Create and present materials for Sponsor meetings
Berufserfahrung
- 3 Jahre
Ausbildung
- Abgeschlossene BerufsausbildungODER
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Benefits
Boni & Prämien
- Bonus
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens Alimentiv 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
Manager Clinical Operations, Single Sponsor(m/w/x)
VollzeitRemoteSeniorFrankfurt am Main - ICON plc
Clinical Site Manager(m/w/x)
VollzeitRemoteSeniorFrankfurt am Main - ICON plc
Clinical Research Lead Assistant(m/w/x)
VollzeitRemoteSeniorFrankfurt am Main - ICON plc
Senior Clinical Research Associate(m/w/x)
Vollzeitmit HomeofficeSeniorFrankfurt am Main
ALAlimentiv
Clinical Operations Lead(m/w/x)
Frankfurt am Main
Vollzeitmit HomeofficeBerufserfahren
Nejo KI-Zusammenfassung
Overseeing clinical project compliance, training, and assessment visits for CRAs. Undergraduate degree and 7-9 years related experience required; Health Sciences, Life Sciences, or Nursing background preferred. Occasional site travel.
Anforderungen
- College diploma/degree
- 7-9 years related experience
- Undergraduate university degree (Bachelors or Honors Bachelors)
- 4-6 years' experience
- Health Sciences, Life Sciences or Nursing specialty preferred
- SoCRA and/or ACRP Certification/Designation
- Minimum of 3 years CRA experience
- Strong experience with EDC systems
- Proficiency with MS Office
- Strong written and verbal communication skills
- Highly effective interpersonal and organizational skills
- Proactivity
- Detail orientation
- Task-driven
- Highly organized
- Understanding of GCPs and local regulations
- Clinical monitoring knowledge
- Ability in report writing
- Strong understanding of clinical research documents
- Ability to handle multiple tasks
- Ability to meet deadlines in a dynamic environment
Aufgaben
- Oversee clinical operations for projects
- Ensure compliance with study protocols and regulations
- Act as a liaison between CRAs and the clinical project team
- Provide project-specific training for CRAs
- Conduct assessment visits with CRAs
- Implement enrollment and recruitment strategies
- Prepare monitoring plans and structural documentation
- Schedule monitoring visits and track performance metrics
- Manage issue escalation and corrective actions
- Develop study tools for site and CRA use
- Review visit reports for quality and compliance
- Track protocol deviations
- Support clinical operations objectives
- Monitor regional CRA compliance with study timelines
- Conduct co-monitoring visits as needed
- Assist in vendor management activities
- Proactively manage site and country performance
- Contribute to financial project management processes
- Manage investigator sites temporarily or permanently
- Conduct regular global CRA calls
- Attend meetings with Study Sponsor for status updates
- Provide operational support to the monitoring team
- Train and mentor regional CRAs on study procedures
- Serve as the first point of contact for CRAs
- Liaise with line managers for CRA assignments
- Conduct CRA assessment visits to evaluate performance
- Develop training materials and study tools
- Create and present materials for Sponsor meetings
Berufserfahrung
- 3 Jahre
Ausbildung
- Abgeschlossene BerufsausbildungODER
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Benefits
Boni & Prämien
- Bonus
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens Alimentiv 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
Associate Manager or Manager, Clinical Operations(m/w/x)
VollzeitRemoteManagementFrankfurt am Main - IQVIA
Manager Clinical Operations, Single Sponsor(m/w/x)
VollzeitRemoteSeniorFrankfurt am Main - ICON plc
Clinical Site Manager(m/w/x)
VollzeitRemoteSeniorFrankfurt am Main - ICON plc
Clinical Research Lead Assistant(m/w/x)
VollzeitRemoteSeniorFrankfurt am Main - ICON plc
Senior Clinical Research Associate(m/w/x)
Vollzeitmit HomeofficeSeniorFrankfurt am Main