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Experienced Clinical Trials Assistant(m/w/x)
Maintenance of Trial Master Files and site compliance tracking for life science research projects. Professional experience in clinical administration and GCP knowledge required. Flexible working schedules, 30 days vacation.
Requirements
- Degree in life science or apprenticeship
- Experience in clinical research administrative roles
- Knowledge of GCP and ICH guidelines
- Fluent German and good English skills
- Proficiency in Microsoft Word, Excel, PowerPoint
- Effective communication and organizational skills
- Independent work and task prioritization
- Flexibility for regular client office visits
Tasks
- Support CRAs and RSU teams with clinical document updates
- Maintain systems like the Trial Master File
- Track site compliance and performance within timelines
- Prepare, handle, and distribute clinical documentation and reports
- File and archive clinical documentation per SOPs
- Perform periodic reviews of study files for completeness
- Prepare and distribute Clinical Trial Supplies
- Maintain tracking information for trial supplies
- Track and manage Case Report Forms and queries
- Manage clinical data flow
- Act as the central contact for project communications
- Manage project correspondence and associated documentation
Education
- High school diploma
Languages
- German – Business Fluent
- English – Business Fluent
Tools & Technologies
- Microsoft Word
- Microsoft Excel
- Microsoft PowerPoint
Benefits
Flexible Working
- Flexible working schedules
- Office and home-office combination
Competitive Pay
- Competitive compensation and benefits
Learning & Development
- Ongoing learning and development
Not a perfect match?
- IQVIAFull-timeWith HomeofficeExperiencedFrankfurt am Main, Hamburg
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Experienced Clinical Trials Assistant(m/w/x)
Maintenance of Trial Master Files and site compliance tracking for life science research projects. Professional experience in clinical administration and GCP knowledge required. Flexible working schedules, 30 days vacation.
Requirements
- Degree in life science or apprenticeship
- Experience in clinical research administrative roles
- Knowledge of GCP and ICH guidelines
- Fluent German and good English skills
- Proficiency in Microsoft Word, Excel, PowerPoint
- Effective communication and organizational skills
- Independent work and task prioritization
- Flexibility for regular client office visits
Tasks
- Support CRAs and RSU teams with clinical document updates
- Maintain systems like the Trial Master File
- Track site compliance and performance within timelines
- Prepare, handle, and distribute clinical documentation and reports
- File and archive clinical documentation per SOPs
- Perform periodic reviews of study files for completeness
- Prepare and distribute Clinical Trial Supplies
- Maintain tracking information for trial supplies
- Track and manage Case Report Forms and queries
- Manage clinical data flow
- Act as the central contact for project communications
- Manage project correspondence and associated documentation
Education
- High school diploma
Languages
- German – Business Fluent
- English – Business Fluent
Tools & Technologies
- Microsoft Word
- Microsoft Excel
- Microsoft PowerPoint
Benefits
Flexible Working
- Flexible working schedules
- Office and home-office combination
Competitive Pay
- Competitive compensation and benefits
Learning & Development
- Ongoing learning and development
About the Company
IQVIA
Industry
Pharmaceuticals
Description
IQVIA is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients.
Not a perfect match?
- IQVIA
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