Senior Clinical Research Associate – Oncology Experience

This is a fully remote position, open to applicants in France.

📋 Description

• Supervise monitoring tasks and the overall execution of the study

• Ensure adherence to regulatory standards, ICH-GCP, and the study protocol

• Execute monitoring procedures utilizing diverse methods (on-site, remote, hybrid)

• Handle reporting and documentation related to protocol deviations

• Confirm the informed consent process and uphold subject confidentiality

⛳️ Requirements

• Experience in clinical trials focused on oncology

• Familiarity with RECIST criteria

• Bachelor’s degree or Registered Nurse (RN) in a relevant field

• Proficiency in the local language

• Advanced or fluent proficiency in English

🏝️ Benefits

• Flexible working arrangements

• Opportunities for professional development

• Collaboration with international teams