Senior Clinical Research Associate – Oncology Experience Required

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

📋 Description

• Supervision of monitoring duties and study execution

• Ensuring compliance with regulatory standards, ICH-GCP guidelines, and study protocols

• Performing reviews of source documents and verifying the accuracy of relevant site source documents and medical records

• Confirming that all required clinical data entered in the Case Report Form (CRF) is both accurate and complete

• Overseeing the reporting of protocol deviations and ensuring appropriate follow-up actions

• Recording activities through follow-up letters, monitoring reports, and communication logs

⛳️ Requirements

• Minimum of 4 years’ experience in CRO or pharmaceutical trial environments

• Experience with oncology trials and knowledge of RECIST criteria

• Strong networking and relationship-building capabilities

• Effective and appropriate communication skills with both internal and external stakeholders

• Proficiency in the local language

• Fluent in English

• Bachelor’s degree or Registered Nurse (RN) in a relevant field or an equivalent combination of education, training, and experience

🏝️ Benefits

• Health insurance

• Opportunities for professional development