Clinical research associate Jobs in Dortmund
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Clinical research associate • dortmund
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Clinical Research Associate
Barrington JamesDortmund, DE- Gesponsert
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Heraeus Medical GmbHDortmund- Gesponsert
SAP FI Senior Manager / Associate Director
MA (Montreal Associates)Dortmund, DE- Gesponsert
Experienced Clinical Research Associate (Sign-On Bonus eligible)
MedpaceDortmund, DEProjektmanager D / A / CH (m / w / d) - IWD market research GmbH
IWD market research GmbHDortmund, DE- Gesponsert
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Gold Group LtdDortmund, DEResearch and Development Project Manager
stellenonline KarriereHerdecke, Germany- Gesponsert
Principal Statistician
Warman O'BrienDortmund, DESenior Data Scientist (m / w / d)
IQVIADortmund, GermanySenior Tax Research Analyst (mw / d)
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KION GroupDortmund, GermanyÄhnliche Suchanfragen
Clinical Research Associate
Barrington JamesDortmund, DEClinical 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.)
- 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
- Proven track record of independently managing monitoring visits
- Strong knowledge of GCP, clinical trial processes, and regulatory requirements
- Confident leading site relationships and supporting trial planning activities
- May support training or mentoring of junior CRAs
- 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
Levels & Experience
CRA I (0–2 years of experience)
CRA II (2–5 years of experience)
Senior CRA (5+ years of experience)
Core Requirements for All Levels