IQVIA
Experienced Clinical Trials Assistant(m/w/x)
Full-timeWith HomeofficeExperienced
Frankfurt am Main
New Job?Nejo!
Your personal AI career agent
IQIQVIA
Experienced Clinical Trials Assistant(m/w/x)
Frankfurt am Main, Hamburg
Full-timeWith Home OfficeExperienced
Nejo AI Summary
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.
Requirements
- 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
Tasks
- 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
Work Experience
- 2 years
Education
- High school diploma
Languages
- German – Business Fluent
- English – Advanced
Tools & Technologies
- Microsoft Word
- Microsoft Excel
- Microsoft PowerPoint
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of IQVIA and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
Not a perfect match?
- 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
Internship in Clinical Research(m/w/x)
Full-timeInternshipWith HomeofficeFrankfurt am Main, Stuttgart - ICON plc
Clinical Trial Assistant(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main
IQIQVIA
Experienced Clinical Trials Assistant(m/w/x)
Frankfurt am Main, Hamburg
Full-timeWith Home OfficeExperienced
Nejo AI Summary
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.
Requirements
- 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
Tasks
- 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
Work Experience
- 2 years
Education
- High school diploma
Languages
- German – Business Fluent
- English – Advanced
Tools & Technologies
- Microsoft Word
- Microsoft Excel
- Microsoft PowerPoint
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of IQVIA and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
About the Company
IQVIA
Industry
Healthcare
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
Experienced Clinical Trials Assistant(m/w/x)
Full-timeWith HomeofficeExperiencedFrankfurt am Main - 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
Internship in Clinical Research(m/w/x)
Full-timeInternshipWith HomeofficeFrankfurt am Main, Stuttgart - ICON plc
Clinical Trial Assistant(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main