수평: Entry level

직업 종류: Full-time

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작업 내용

The Clinical Research Associate (CRA) works under the hierarchical supervision of the Head of Monitoring.

Main responsibilities / Major Activities

The CRA is responsible for “on-site” monitoring of clinical trial to ensure that it is conducted, recorded and reported in accordance with the protocol, the principles of Good Clinical Practice (GCP) and the applicable regulatory requirements.

Clinical monitoring is integrated in a multi-step process involving close cooperation between the participating investigators, research nurses, and other site scientists involved in the clinical trial.

  • Perform on-site monitoring visits to EORTC participating institutions according to the monitoring plan and following the EORTC Standard Operating procedures (SOPs) and GCP guidelines.
  • Ensures and control sites’ compliance with study protocol and associated guidelines
  • Address issues in a manner that is beneficial for the site and the EORTC team.
  • Support the site’s staffs to reach better quality level, as needed.
  • Report the findings of the on-site monitoring visits according to EORTC Standards.
  • Follow the sites’ findings until resolution with the support of EORTC study team and Monitoring department staff, as appropriate.
  • Perform site’s training before and/or during the study conduct, as required.

Profile

  • University degree or equivalent in Health Sciences
  • Prior experience in Oncology
  • Excellent verbal and written communication skills
  • Excellent organization skills
  • Proactivity and dynamism
  • Flexibility in respect to work assignments and new learnings
  • Ability to travel 40% of working time across European countries.
  • Languages:
    • English (written & spoken) is mandatory.
    • Knowledge of other language(s) is an asset.
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마감 시간: 20-01-2026

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