Senior Oncology CRA — Independent Site Monitor

ThermoFisher Scientific; Santiago; On-site; CLP 18,000,000 - 24,000,000; Full time

Job summary

Thermo Fisher Scientific is seeking a Senior Clinical Research Associate with oncology expertise to monitor study sites across multiple phases and ensure compliance with ICH-GCP and AZ SOPs. The role requires 3–5 years of monitoring experience, independence, and the ability to travel internationally.

A valid driving license is required. The SrCRA will collaborate with the Local Study Team to deliver study commitments on time, manage site initiation, monitoring, and closure activities, and

Qualifications

• Minimum 3–5 years of experience as a Clinical Research Associate (monitor)
• Special therapeutic expertise in oncology
• Willingness and ability to travel internationally
• Valid driving license required

Responsibilities

• Lead site monitoring activities and ensure study compliance according to ICH-GCP and AZ SOPs.
• Coordinate with Local Study Team and LSAD to deliver study commitments on time.
• Prepare and finalize monitoring visit reports and follow up on actions.
• Ensure timely data entry and query resolution in CTMS and other systems.
• Maintain inspection readiness and support audits/regulatory inspections.

Skills

Monitoring

Oncology

Travel flexibility

Driving license

Job description

Thermo Fisher Scientific is seeking a Senior Clinical Research Associate with oncology expertise to monitor study sites across multiple phases and ensure compliance with ICH-GCP and AZ SOPs. The role requires 3–5 years of monitoring experience, independence, and the ability to travel internationally.

A valid driving license is required. The SrCRA will collaborate with the Local Study Team to deliver study commitments on time, manage site initiation, monitoring, and closure activities, and