CRA Automatizador de Pruebas Clínicas

Kabeli Selección; Santiago; On-site; CLP 9,000,000 - 13,000,000; Full time

Job summary

Kabeli Selección is seeking a Clinical Research Associate (CRA) to oversee study activities at allocated sites and collaborate with local study teams. The CRA will monitor study conduct, ensure timely delivery, and act as the main site contact, supporting regulatory compliance with ICH-GCP guidelines.

The role requires 0–2 years of relevant experience, English proficiency, and a degree in a scientific or health-related field.

Qualifications

• 0–2 years of prior relevant experience in clinical research.
• Good knowledge of regulatory requirements such as GCP and ICH.
• Strong written and verbal English communication skills.

Responsibilities

• Participates as the local CRA in monitoring assignments to ensure timely study delivery.
• Prepares, initiates, monitors and closes study sites per protocol and regulatory requirements.
• Ensures data quality, safety reporting, and regulatory compliance during site visits and remote monitoring.
• Maintains CTMS data and liaises with LSAD and study teams to support site performance.
• Supports audits and regulatory inspections in liaison with local management.

Skills

0-2 years experience

GCP/ICH knowledge

English language

Education

Degree in scientific discipline or health care

Job description

Kabeli Selección is seeking a Clinical Research Associate (CRA) to oversee study activities at allocated sites and collaborate with local study teams. The CRA will monitor study conduct, ensure timely delivery, and act as the main site contact, supporting regulatory compliance with ICH-GCP guidelines.

The role requires 0–2 years of relevant experience, English proficiency, and a degree in a scientific or health-related field.