Clinical Study Coordinator (Medical Oncology and Hematology) | Studienkoordinator:in (w/m/d) in der Klinik für Medizinische Onkologie und Hämatologie 80-100%

Universitätsspital Zürich

Zürich, ZH, Switzerland
Published Dec 12, 2025
Part-time
Permanent

Job Summary

This dynamic and varied role as a Clinical Study Coordinator in Medical Oncology and Hematology places you at the heart of clinical trial processes at one of Switzerland's largest hospitals. Serving as the central interface, you will ensure all study procedures are clearly structured, transparently communicated, and implemented smoothly, working closely with medical, nursing, and laboratory teams, as well as external sponsors and CROs. A core focus of the role is comprehensive data management, including structured data capture, maintenance, and meticulous GCP-compliant documentation of all processes (ISF/TMF). Furthermore, you will manage contractual agreements, support budget planning, coordinate logistics for study medications and samples, and handle study invoicing. This position demands strong organizational skills, proactive problem-solving, and effective communication to navigate interdisciplinary collaboration and changing priorities, offering an exciting path for those wishing to actively shape a dynamic research environment.

Required Skills

Education

Vocational training or B.Sc / M.Sc degree in a medical or natural science field

Experience

  • Professional experience in conducting clinical studies
  • Proven knowledge of GCP and a recognized Swiss (CH) certification
  • Knowledge of medical terminology, physiology, and pathophysiology in the hematological/oncological area
  • Experience managing contracts, budgeting, and study invoicing

Languages

German (Fluent)English (Fluent)

Additional

  • Must possess a reliable, proactive, and solution-oriented work style with excellent organizational skills, and the ability to manage multiple responsibilities and deadlines.