IQVIA
Experienced Clinical Trials Assistant(m/w/x)
Vollzeitmit HomeofficeBerufserfahren
Frankfurt am Main, Hamburg
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IQIQVIA
Experienced Clinical Trial Coordinator(m/w/x)
Frankfurt am Main
Vollzeitmit HomeofficeBerufserfahren
Nejo KI-Zusammenfassung
Coordinating clinical documentation, trial supplies, and data flow in human data science projects. Fluent German C1 and GCP/ICH guidelines knowledge required. Home-Office throughout Germany.
Anforderungen
- Bachelor’s or higher-level degree in life science or High School Diploma and apprenticeship in life science, medical or pharmaceutical field, or office management
- At least 2-4 years experience as Clinical Trial Coordinator or in another administrative role in clinical research
- Knowledge of clinical research regulatory requirements, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Fluent in German at C1 level and good command of English
- Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint
- Effective communication, organizational and planning skills
- Ability to work independently and prioritize tasks while working on multiple projects
- Ability to establish and maintain effective working relationships with coworkers, managers and clients
Aufgaben
- Assist Clinical Research Associates with updating and maintaining clinical documents
- Collaborate on the preparation and distribution of clinical documentation and reports
- Review study files for completeness
- Coordinate the management of Clinical Trial Supplies and tracking information
- Manage the tracking of Case Report Forms and clinical data flow
- Serve as a central contact for project communications and documentation
- Mentor less experienced Clinical Trial Coordinators and assist with training
- Act as a subject matter expert for business processes
- Participate in quality or process improvement initiatives
Berufserfahrung
- 2 - 4 Jahre
Ausbildung
- Matura
Sprachen
- Deutsch – verhandlungssicher
- Englisch – fortgeschritten
Tools & Technologien
- Microsoft Word
- Microsoft Excel
- Microsoft PowerPoint
Benefits
Attraktive Vergütung
- Competitive salary and benefits package
Mentoring & Coaching
- In-depth training and mentoring
Flexibles Arbeiten
- Home-Office throughout Germany
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens IQVIA 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
Experienced Clinical Trials Assistant(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenFrankfurt am Main - IQVIA
Global Clinical Trial Coordinator(m/w/x)
Vollzeitmit HomeofficeSeniorFrankfurt am Main - IQVIA
Study Site Management Specialist(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenFrankfurt am Main - IQVIA RDS GmbH
Clinical Trial Manager - Single Sponsor dedicated(m/w/x)
VollzeitRemoteBerufserfahrenFrankfurt am Mainab 70.100 / Jahr
IQIQVIA
Experienced Clinical Trial Coordinator(m/w/x)
Frankfurt am Main
Vollzeitmit HomeofficeBerufserfahren
Nejo KI-Zusammenfassung
Coordinating clinical documentation, trial supplies, and data flow in human data science projects. Fluent German C1 and GCP/ICH guidelines knowledge required. Home-Office throughout Germany.
Anforderungen
- Bachelor’s or higher-level degree in life science or High School Diploma and apprenticeship in life science, medical or pharmaceutical field, or office management
- At least 2-4 years experience as Clinical Trial Coordinator or in another administrative role in clinical research
- Knowledge of clinical research regulatory requirements, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Fluent in German at C1 level and good command of English
- Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint
- Effective communication, organizational and planning skills
- Ability to work independently and prioritize tasks while working on multiple projects
- Ability to establish and maintain effective working relationships with coworkers, managers and clients
Aufgaben
- Assist Clinical Research Associates with updating and maintaining clinical documents
- Collaborate on the preparation and distribution of clinical documentation and reports
- Review study files for completeness
- Coordinate the management of Clinical Trial Supplies and tracking information
- Manage the tracking of Case Report Forms and clinical data flow
- Serve as a central contact for project communications and documentation
- Mentor less experienced Clinical Trial Coordinators and assist with training
- Act as a subject matter expert for business processes
- Participate in quality or process improvement initiatives
Berufserfahrung
- 2 - 4 Jahre
Ausbildung
- Matura
Sprachen
- Deutsch – verhandlungssicher
- Englisch – fortgeschritten
Tools & Technologien
- Microsoft Word
- Microsoft Excel
- Microsoft PowerPoint
Benefits
Attraktive Vergütung
- Competitive salary and benefits package
Mentoring & Coaching
- In-depth training and mentoring
Flexibles Arbeiten
- Home-Office throughout Germany
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens IQVIA 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
IQVIA
Branche
Healthcare
Beschreibung
IQVIA is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients.
Noch nicht perfekt?
- IQVIA
Experienced Clinical Trials Assistant(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenFrankfurt am Main, Hamburg - IQVIA
Experienced Clinical Trials Assistant(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenFrankfurt am Main - IQVIA
Global Clinical Trial Coordinator(m/w/x)
Vollzeitmit HomeofficeSeniorFrankfurt am Main - IQVIA
Study Site Management Specialist(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenFrankfurt am Main - IQVIA RDS GmbH
Clinical Trial Manager - Single Sponsor dedicated(m/w/x)
VollzeitRemoteBerufserfahrenFrankfurt am Mainab 70.100 / Jahr