Clinical Research Associate
Eckdaten der angebotenen Stelle
| Arbeitgeber | Barrington James |
| Postleitzahl | |
| Ort | Düsseldorf |
| Bundesland | Nordrhein-Westfalen |
| Gepostet am | 27.06.2025 |
| Remote Option? | - |
| Homeoffice Option? | - |
| Teilzeit? | - |
| Vollzeit? | - |
| Ausbildungsstelle? | - |
| Praktikumsplatz?? | - |
| Unbefristet? | - |
| Befristet? | - |
Stellenbeschreibung
*YOU MUST BE BASED IN GERMANY TO APPLY**YOU MUST HAVE CRA EXPEREINCE*
Clinical Research Associate – Germany (Remote or Office-Based)
CRA (Entry-Level to Senior CRA) – Multiple Openings
We’re hiring Clinical Research Associates at three levels to support a portfolio of international clinical trials. These are permanent roles based in Germany, with the flexibility to work fully remote or from an office.
If you’re early in your CRA career or bring years of site monitoring expertise, we’d love to hear from you.
About the Role
You’ll play a central part in the execution of clinical studies, supporting patient safety, protocol adherence, and data integrity across a variety of therapeutic areas.
Key Responsibilities
Levels & Experience
CRA I (1–2 years of experience)
CRA II (2–5 years of experience)
Senior CRA (5+ years of experience)
Core Requirements for All Levels
To apply
nfordyce@barringtonjames.com
Clinical Research Associate – Germany (Remote or Office-Based)
CRA (Entry-Level to Senior CRA) – Multiple Openings
We’re hiring Clinical Research Associates at three levels to support a portfolio of international clinical trials. These are permanent roles based in Germany, with the flexibility to work fully remote or from an office.
If you’re early in your CRA career or bring years of site monitoring expertise, we’d love to hear from you.
About the Role
You’ll play a central part in the execution of clinical studies, supporting patient safety, protocol adherence, and data integrity across a variety of therapeutic areas.
Key Responsibilities
- Conducting site qualification, initiation, routine monitoring, and close-out visits
- Ensuring compliance with ICH-GCP, protocol requirements, and local regulations
- Liaising with investigators and study site teams to ensure smooth trial conduct
- Performing source data verification, addressing queries, and maintaining quality standards
- Supporting the review of clinical study documentation (protocols, reports, etc.)
Levels & Experience
CRA I (1–2 years of experience)
- Ideally some exposure to site monitoring or clinical operations (e.g. CTA or junior CRA background)
- Strong organisational skills and willingness to learn in a fast-paced environment
CRA II (2–5 years of experience)
- Proven track record of independently managing monitoring visits
- Strong knowledge of GCP, clinical trial processes, and regulatory requirements
Senior CRA (5+ years of experience)
- Confident leading site relationships and supporting trial planning activities
- May support training or mentoring of junior CRAs
Core Requirements for All Levels
- Bachelor’s degree in a life sciences, nursing, pharmacy, or healthcare-related field
- Fluency in German and English
- Willingness to travel for on-site visits
- A strong commitment to quality, compliance, and collaboration
To apply
nfordyce@barringtonjames.com