CRA II/Sr CRA based in Berlin or Hamburg
HybridBerlin, State of Berlin, Germany or Hamburg, Hamburg, Germany
Job Summary
CRA II/Sr CRA based in Berlin or Hamburg performs site qualification, site initiation, interim monitoring, site management and close-out visits (on-site or remotely), ensures regulatory and ICH-GCP/GPP compliance, verifies informed consent, monitors data quality and IP handling, conducts source data review, supports recruitment and retention strategies, and collaborates with cross-functional teams to ensure trial integrity and patient safety. Requires German and English proficiency, bachelor’s degree or nursing background, and ability to travel up to 75% within Germany.
Required Qualifications
- Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience; knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements; previous monitoring experience in Germany; Phase I experience would be a plus; fluency in German and proficiency in English; ability to travel up to 75% and reside in the North-Eastern region of the country.
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