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ARTIDISPosted 3 weeks ago

Clinical Scientist (Medical Focus)

On-siteBasel, Basel-City, Switzerland

Full TimeDoctorate Or Professional DegreeSmall

Job Summary

Conduct on-site clinical and pathological data collection at ARTIDIS study locations in the Basel area, collaborating with investigators, surgeons, and pathologists to verify information in electronic data capture platforms. Review Case Report Forms for medical coherence, perform structured data quality checks to identify inconsistencies, and translate source documents into analysis-ready entries. Support medically informed data reviews to resolve queries and provide clinical context for dataset interpretation alongside analysts and statisticians. Requires an MD or equivalent medical qualification with oncology focus, fluency in German and English, and regular presence at hospital sites. Fluency in German and English, both written and spoken.

Required Qualifications

  • Medical degree (MD, any specialty), medical laboratory scientist or bio analyst qualification, or a comparable medical or health-science background with strong clinical or pathology exposure
  • Clinical research experience, including contributing to a data lock or database closure event
  • Hands-on experience in a hospital, clinical laboratory, pathology, or comparable clinical environment and confidence to collaborate with clinical site personnel
  • A practical understanding of how clinical and pathological data are generated, documented, reviewed, and interpreted
  • Ability to evaluate protocols and CRFs from a medical perspective, or strong transferable experience that demonstrates the ability to do so
  • Fluency in German and English, both written and spoken
  • Strong analytical judgment, attention to detail, and a structured, hands-on approach to data quality and problem solving

Desired Qualifications

  • An oncology focus
  • Familiarity with Good Clinical Practice and ICH E6 principles
  • Experience in pathology or histology and confidence in reading and interpreting pathology reports
  • Experience with oncology clinical trials or studies involving medical devices or in vitro diagnostics
  • Experience with EDC/eCRF systems, clinical data review, data query management, or clinical data management processes

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