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Experienced Clinical Trials Assistant(m/w/x)
Description
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.
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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
Education
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
Tools & Technologies
Languages
German – Business Fluent
English – Business Fluent
Benefits
Flexible Working
- •Flexible working schedules
- •Office and home-office combination
Competitive Pay
- •Competitive compensation and benefits
Learning & Development
- •Ongoing learning and development
- IQVIAFull-timeWith HomeofficeExperiencedFrankfurt am Main, Hamburg
- IQVIA
Experienced Clinical Trial Coordinator(m/w/x)
Full-timeWith HomeofficeExperiencedFrankfurt am Main - IQVIA
Clinical Trials Assistant 1(m/w/x)
Full-time/Part-timeWith HomeofficeNot specifiedFrankfurt am Main - IQVIA RDS GmbH
Experienced Clinical Research Associate, Multi-Sponsor(m/w/x)
Full-timeWith HomeofficeExperiencedFrankfurt am Main - IQVIA
Global Clinical Trial Coordinator(m/w/x)
Full-timeWith HomeofficeSeniorFrankfurt am Main
Experienced Clinical Trials Assistant(m/w/x)
The AI Job Search Engine
Description
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.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
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
Education
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
Tools & Technologies
Languages
German – Business Fluent
English – Business Fluent
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.
- IQVIA
Experienced Clinical Trials Assistant(m/w/x)
Full-timeWith HomeofficeExperiencedFrankfurt am Main, Hamburg - IQVIA
Experienced Clinical Trial Coordinator(m/w/x)
Full-timeWith HomeofficeExperiencedFrankfurt am Main - IQVIA
Clinical Trials Assistant 1(m/w/x)
Full-time/Part-timeWith HomeofficeNot specifiedFrankfurt am Main - IQVIA RDS GmbH
Experienced Clinical Research Associate, Multi-Sponsor(m/w/x)
Full-timeWith HomeofficeExperiencedFrankfurt am Main - IQVIA
Global Clinical Trial Coordinator(m/w/x)
Full-timeWith HomeofficeSeniorFrankfurt am Main