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Senior CRA I/II - Senior Klinischer Monitor (m/w/d)
Hybrid · Karlsruhe, Baden-Wurttemberg, Germany
Job Summary
In this role, experienced Clinical Research Associates with 2+ years of independent monitoring experience are needed to manage clinical trial sites across Germany, focusing on compliance with protocols, ICH-GCP, and regulations. Responsibilities include conducting monitoring activities (both on-site and remote), maintaining audit readiness, documenting activities in timely reports, and communicating effectively with investigators and site staff. Candidates must possess strong clinical monitoring skills, a Bachelor’s degree in life sciences, and fluency in German and English.
Required Qualifications
- Minimum 2+ years of experience as a Clinical Research Associate / Monitor
- Bachelor’s degree in a life sciences related field or equivalent qualification
- Valid driver’s license
- Full right to work in Germany
- Fluency in German and English (C1 level)
Desired Qualifications
- Strong clinical monitoring skills with hands-on RBM experience
- Solid therapeutic area knowledge and medical terminology
- Well-developed critical thinking, problem-solving, and root cause analysis skills
- Strong written and verbal communication skills with medical professionals
- High attention to detail and strong organizational skills
- Flexibility and adaptability in a dynamic project environment
- Proficiency in Microsoft Office and ability to learn clinical systems (e.g., CTMS)
Additional Requirements
- Severely disabled applicants with the same aptitude will be given preferential treatment.
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