IQVIA
Experienced Clinical Trials Assistant(m/w/x)
Vollzeitmit HomeofficeBerufserfahren
Frankfurt am Main
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IQIQVIA
Experienced Clinical Trials Assistant(m/w/x)
Frankfurt am Main, Hamburg
Vollzeitmit HomeofficeBerufserfahren
Nejo KI-Zusammenfassung
Managing documentation, supplies, and data flow for human data science projects. 2+ years research admin experience and excellent GCP/ICH knowledge required. Support for global research projects.
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
- 2 years or more of experience as Clinical Trials Assistant or in another administrative role in clinical research, or at least 3 years experience as working student in clinical research
- Excellent knowledge of clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Fluent language skills in German on at least 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 effectively prioritize tasks
- Flexibility to visit client's office for meetings in Hamburg area 2-3 days/week or according to an agreed schedule
Aufgaben
- Assist Clinical Research Associates with updating and maintaining clinical documents
- Support the clinical team in preparing, handling, and archiving clinical documentation
- Conduct periodic reviews of study files for completeness
- Help with the distribution and tracking of Clinical Trial Supplies
- Manage Case Report Forms, queries, and clinical data flow
- Serve as a central contact for project communications and documentation
- Accompany CRAs on site visits to assist with clinical monitoring duties
Berufserfahrung
- 2 Jahre
Ausbildung
- Matura
Sprachen
- Deutsch – verhandlungssicher
- Englisch – fortgeschritten
Tools & Technologien
- Microsoft Word
- Microsoft Excel
- Microsoft PowerPoint
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.
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VollzeitRemoteBerufserfahrenFrankfurt am Main
IQIQVIA
Experienced Clinical Trials Assistant(m/w/x)
Frankfurt am Main, Hamburg
Vollzeitmit HomeofficeBerufserfahren
Nejo KI-Zusammenfassung
Managing documentation, supplies, and data flow for human data science projects. 2+ years research admin experience and excellent GCP/ICH knowledge required. Support for global research projects.
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
- 2 years or more of experience as Clinical Trials Assistant or in another administrative role in clinical research, or at least 3 years experience as working student in clinical research
- Excellent knowledge of clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Fluent language skills in German on at least 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 effectively prioritize tasks
- Flexibility to visit client's office for meetings in Hamburg area 2-3 days/week or according to an agreed schedule
Aufgaben
- Assist Clinical Research Associates with updating and maintaining clinical documents
- Support the clinical team in preparing, handling, and archiving clinical documentation
- Conduct periodic reviews of study files for completeness
- Help with the distribution and tracking of Clinical Trial Supplies
- Manage Case Report Forms, queries, and clinical data flow
- Serve as a central contact for project communications and documentation
- Accompany CRAs on site visits to assist with clinical monitoring duties
Berufserfahrung
- 2 Jahre
Ausbildung
- Matura
Sprachen
- Deutsch – verhandlungssicher
- Englisch – fortgeschritten
Tools & Technologien
- Microsoft Word
- Microsoft Excel
- Microsoft PowerPoint
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 - IQVIA
Experienced Clinical Trial Coordinator(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenFrankfurt am Main - IQVIA
Clinical Trials Assistant 1(m/w/x)
Vollzeit/Teilzeitmit HomeofficeKeine AngabeFrankfurt am Main - IQVIA RDS GmbH
Internship in Clinical Research(m/w/x)
VollzeitPraktikummit HomeofficeFrankfurt am Main, Stuttgart - ICON plc
Clinical Trial Assistant(m/w/x)
VollzeitRemoteBerufserfahrenFrankfurt am Main