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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
Work Experience
- approx. 1 - 4 years
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
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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
Work Experience
- approx. 1 - 4 years
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
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
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.
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