Clinical Research Associate

  • permanent
  • Geneva


The CRA is primarily responsible for supporting the clinical studies and for clinical study management:

  • Prepares the study sites for site initiation.
  • Develops the monitoring plan and related documents.
  • Supports the regulatory submission process.
  • Conducts site initiation, monitoring and site closure, ensuring the documentation is maintained.
  • Supports the development of a patient enrolment plan and investigates patient enrolment delays.
  • Oversees safety reporting, tracks study reported adverse events, writes safety narratives, coordinate safety reviews.
  • Supports Clinical Study Coordinator as needed (contracts, TMF, invoices, etc)


  • Registered Nurse or equivalent medical background or bachelor’s degree in a healthcare or other life sciences discipline.
  • Experience in clinical study monitoring on-site.
  • Knowledge and experience of Good Clinical Practice relating to medical device studies.
  • Excellent communication and collaboration skills.
  • A high sense of responsibility and reliability.
  • Competent in English and French, and additional skills in Spanish.
  • Flexibility to travel intermittently up to 30%.