IQVIA RDS GmbH
Internship in Clinical Research(m/w/x)
Full-timeInternshipWith Homeoffice
Frankfurt am Main
New Job?Nejo!
The AI Job Search Engine
IQIQVIA
Trainee Clinical Research Associate(m/w/x)
Frankfurt am Main
Full-timeWith Home Office
Nejo AI Summary
Managing clinical trial site visits, documentation, and training at a human data science company. Advanced clinical research training and German C1 proficiency required. Home-Office in Germany, flexible schedule, and mentoring support.
Requirements
- Degree in health care, science, or medical vocational education
- Advanced training in clinical research
- German C1 level and good English command
- Flexibility for regular travel and driving license
- Proficiency in Microsoft Word, Excel, and PowerPoint
- Excellent organizational and problem-solving skills
- Effective time management and priority management
- Ability to maintain effective working relationships
- Availability to start on 1.Mar.2026
Tasks
- Perform site selection, initiation, monitoring, and close-out visits
- Maintain appropriate documentation for all site visits
- Support the development of subject recruitment plans
- Establish regular lines of communication with assigned sites
- Administer protocol and related study training to site staff
- Evaluate the quality and integrity of site practices
- Escalate quality issues through the appropriate channels
- Track regulatory submissions and recruitment progress
- Manage case report form completion and data query resolution
Education
- Vocational certificationOR
- Bachelor's degree
Languages
- German – Business Fluent
- English – Business Fluent
Tools & Technologies
- Microsoft Word
- Microsoft Excel
- Microsoft PowerPoint
Benefits
Job Security
- Permanent employment contract
Flexible Working
- Home-Office in Germany
- Flexible working schedule
Learning & Development
- In-depth training
Mentorship & Coaching
- Mentoring and co-monitoring
Company Vehicle
- Company car
Other Benefits
- Accident insurance
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?
- ICON plc
(Senior) Clinical Research Associate (CRA) - sponsor dedicated(m/w/x)
Full-timeRemoteNot specifiedFrankfurt am Main - IQVIA RDS GmbH
Internship in Clinical Research(m/w/x)
Full-timeInternshipWith HomeofficeFrankfurt am Main, Stuttgart - ICON plc
Clinical Research Associate (CRA)(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main - IQVIA RDS GmbH
Experienced Clinical Research Associate, Multi-Sponsor(m/w/x)
Full-timeWith HomeofficeExperiencedFrankfurt am Main
IQIQVIA
Trainee Clinical Research Associate(m/w/x)
Frankfurt am Main
Full-timeWith Home Office
Nejo AI Summary
Managing clinical trial site visits, documentation, and training at a human data science company. Advanced clinical research training and German C1 proficiency required. Home-Office in Germany, flexible schedule, and mentoring support.
Requirements
- Degree in health care, science, or medical vocational education
- Advanced training in clinical research
- German C1 level and good English command
- Flexibility for regular travel and driving license
- Proficiency in Microsoft Word, Excel, and PowerPoint
- Excellent organizational and problem-solving skills
- Effective time management and priority management
- Ability to maintain effective working relationships
- Availability to start on 1.Mar.2026
Tasks
- Perform site selection, initiation, monitoring, and close-out visits
- Maintain appropriate documentation for all site visits
- Support the development of subject recruitment plans
- Establish regular lines of communication with assigned sites
- Administer protocol and related study training to site staff
- Evaluate the quality and integrity of site practices
- Escalate quality issues through the appropriate channels
- Track regulatory submissions and recruitment progress
- Manage case report form completion and data query resolution
Education
- Vocational certificationOR
- Bachelor's degree
Languages
- German – Business Fluent
- English – Business Fluent
Tools & Technologies
- Microsoft Word
- Microsoft Excel
- Microsoft PowerPoint
Benefits
Job Security
- Permanent employment contract
Flexible Working
- Home-Office in Germany
- Flexible working schedule
Learning & Development
- In-depth training
Mentorship & Coaching
- Mentoring and co-monitoring
Company Vehicle
- Company car
Other Benefits
- Accident insurance
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
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 RDS GmbH
Internship in Clinical Research(m/w/x)
Full-timeInternshipWith HomeofficeFrankfurt am Main - ICON plc
(Senior) Clinical Research Associate (CRA) - sponsor dedicated(m/w/x)
Full-timeRemoteNot specifiedFrankfurt am Main - IQVIA RDS GmbH
Internship in Clinical Research(m/w/x)
Full-timeInternshipWith HomeofficeFrankfurt am Main, Stuttgart - ICON plc
Clinical Research Associate (CRA)(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main - IQVIA RDS GmbH
Experienced Clinical Research Associate, Multi-Sponsor(m/w/x)
Full-timeWith HomeofficeExperiencedFrankfurt am Main