The AI Job Search Engine
Experienced Clinical Trial Coordinator(m/w/x)
Coordinating clinical documentation, trial supplies, and data flow in human data science projects. Fluent German C1 and GCP/ICH guidelines knowledge required. Home-Office throughout Germany.
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
- At least 2-4 years experience as Clinical Trial Coordinator or in another administrative role in clinical research
- Knowledge of clinical research regulatory requirements, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Fluent in German at 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 prioritize tasks while working on multiple projects
- Ability to establish and maintain effective working relationships with coworkers, managers and clients
Tasks
- Assist Clinical Research Associates with updating and maintaining clinical documents
- Collaborate on the preparation and distribution of clinical documentation and reports
- Review study files for completeness
- Coordinate the management of Clinical Trial Supplies and tracking information
- Manage the tracking of Case Report Forms and clinical data flow
- Serve as a central contact for project communications and documentation
- Mentor less experienced Clinical Trial Coordinators and assist with training
- Act as a subject matter expert for business processes
- Participate in quality or process improvement initiatives
Work Experience
- 2 - 4 years
Education
- High school diploma
Languages
- German – Business Fluent
- English – Advanced
Tools & Technologies
- Microsoft Word
- Microsoft Excel
- Microsoft PowerPoint
Benefits
Competitive Pay
- Competitive salary and benefits package
Mentorship & Coaching
- In-depth training and mentoring
Flexible Working
- Home-Office throughout Germany
Not a perfect match?
- IQVIAFull-timeWith HomeofficeExperiencedFrankfurt am Main, Hamburg
- IQVIA
Experienced Clinical Trials Assistant(m/w/x)
Full-timeWith HomeofficeExperiencedFrankfurt am Main - IQVIA
Global Clinical Trial Coordinator(m/w/x)
Full-timeWith HomeofficeSeniorFrankfurt am Main - IQVIA
Study Site Management Specialist(m/w/x)
Full-timeWith HomeofficeExperiencedFrankfurt am Main - IQVIA RDS GmbH
Clinical Trial Manager - Single Sponsor dedicated(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Mainfrom 70,100 / year
Experienced Clinical Trial Coordinator(m/w/x)
Coordinating clinical documentation, trial supplies, and data flow in human data science projects. Fluent German C1 and GCP/ICH guidelines knowledge required. Home-Office throughout Germany.
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
- At least 2-4 years experience as Clinical Trial Coordinator or in another administrative role in clinical research
- Knowledge of clinical research regulatory requirements, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Fluent in German at 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 prioritize tasks while working on multiple projects
- Ability to establish and maintain effective working relationships with coworkers, managers and clients
Tasks
- Assist Clinical Research Associates with updating and maintaining clinical documents
- Collaborate on the preparation and distribution of clinical documentation and reports
- Review study files for completeness
- Coordinate the management of Clinical Trial Supplies and tracking information
- Manage the tracking of Case Report Forms and clinical data flow
- Serve as a central contact for project communications and documentation
- Mentor less experienced Clinical Trial Coordinators and assist with training
- Act as a subject matter expert for business processes
- Participate in quality or process improvement initiatives
Work Experience
- 2 - 4 years
Education
- High school diploma
Languages
- German – Business Fluent
- English – Advanced
Tools & Technologies
- Microsoft Word
- Microsoft Excel
- Microsoft PowerPoint
Benefits
Competitive Pay
- Competitive salary and benefits package
Mentorship & Coaching
- In-depth training and mentoring
Flexible Working
- Home-Office throughout Germany
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, Hamburg - IQVIA
Experienced Clinical Trials Assistant(m/w/x)
Full-timeWith HomeofficeExperiencedFrankfurt am Main - IQVIA
Global Clinical Trial Coordinator(m/w/x)
Full-timeWith HomeofficeSeniorFrankfurt am Main - IQVIA
Study Site Management Specialist(m/w/x)
Full-timeWith HomeofficeExperiencedFrankfurt am Main - IQVIA RDS GmbH
Clinical Trial Manager - Single Sponsor dedicated(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Mainfrom 70,100 / year