CRA Senior - Coordinación de Ensayos Clínicos

Grupo Progestion; Santiago; On-site; CLP 18,000,000 - 28,000,000; Full time

Job summary

Thermo Fisher Scientific is seeking a Clinical Research Associate (CRA) level II for our Santiago, Chile operations. The role focuses on delivering contracted study activities at allocated sites, coordinating with the local study team, and ensuring compliance with GCP/ICH guidelines and AZ procedures.

Responsibilities include site initiation, monitoring, and closeout to support study timelines. The CRA will work with senior staff and LSAD to maintain site performance, train site personnel, and

Qualifications

• 0-2 years of prior relevant experience.
• Good knowledge of clinical research regulatory requirements (GCP/ICH).
• Strong written and verbal English communication.

Responsibilities

• Prepare, initiate, monitor and close study sites in clinical studies.
• Ensure study commitments are achieved in a timely and efficient manner with the local study team.
• Maintain site readiness and regulatory compliance per ICH-GCP and AZ SOPs.

Skills

Experience level

GCP knowledge

ICH guidelines

English communication

Education

Science/Healthcare degree

Job description

Thermo Fisher Scientific is seeking a Clinical Research Associate (CRA) level II for our Santiago, Chile operations. The role focuses on delivering contracted study activities at allocated sites, coordinating with the local study team, and ensuring compliance with GCP/ICH guidelines and AZ procedures.

Responsibilities include site initiation, monitoring, and closeout to support study timelines. The CRA will work with senior staff and LSAD to maintain site performance, train site personnel, and