Senior Clinical Research Associate – Oncology Experience Required

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

📋 Description

• Ensure adherence to ICH GCP and local regulations at the site level

• Perform monitoring activities both on-site and remotely

• Work collaboratively with the Site Manager and site personnel

• Oversee data integrity and quality assurance

• Execute source document review and verification

⛳️ Requirements

• Over 4 years of experience in CRO or Pharmaceutical trial environments

• Experience with oncology trials and RECIST criteria

• Bachelor's degree or Registered Nurse (RN) in a related field or equivalent

• Demonstrated ability to communicate effectively with stakeholders

• Proficiency in the local language and fluency in English are required

🏝️ Benefits

• Health insurance

• 401(k) plan

• Paid time off

• Flexible work arrangements