Clinical Research Associate (CRA) – Start-Up & Monitoring

Viña Concha y Toro; Santiago; On-site; CLP 25,000,000 - 35,000,000; Full time

Job summary

Thermo Fisher Scientific in Santiago, Chile, seeks a Clinical Research Associate (CRA) Level II (FSP) to manage local study delivery at assigned sites. You will work with the local study team to ensure timely initiation, monitoring and closure of sites in compliance with ICH-GCP and AZ SOPs.

This entry-level to early-career CRA role requires up to 2 years of experience, strong regulation knowledge, and solid English communication.

Qualifications

• Familiarity with Good Clinical Practice (GCP) and ICH guidelines.
• Knowledge of clinical research regulatory requirements and documentation.
• Proficient written and verbal English communication.

Responsibilities

• Monitor and manage site activities to ensure study commitments are met.
• Prepare, initiate, monitor, and close study sites in line with ICH-GCP and AZ SOPs.
• Collaborate with Local Study Team and LSAD to maintain study timelines and site performance.
• Contribute to training, regulatory submissions, and site readiness for audits and inspections.

Skills

GCP/ICH familiarity

Clinical research regulatory knowledge

English communication

Education

Science/healthcare degree

Job description

Thermo Fisher Scientific in Santiago, Chile, seeks a Clinical Research Associate (CRA) Level II (FSP) to manage local study delivery at assigned sites. You will work with the local study team to ensure timely initiation, monitoring and closure of sites in compliance with ICH-GCP and AZ SOPs.

This entry-level to early-career CRA role requires up to 2 years of experience, strong regulation knowledge, and solid English communication.