Junior CRA: Site Monitoring & Compliance

ThermoFisher Scientific; Chile; Remote; CLP 31,434,000 - 51,081,000; Full time

Job summary

Thermo Fisher Scientific is seeking a Clinical Research Associate (CRA) to manage monitoring at allocated sites and collaborate with local study teams. You will ensure compliance with ICH-GCP, regulatory requirements, and study commitments, delivering high-quality data and site oversight.

Ideal candidates have 0-2 years of relevant experience, a degree in science/healthcare, and strong English communication skills.

Qualifications

• 0-2 years of prior relevant experience.
• Good knowledge of GCP/ICH.
• Strong written and verbal English communication.

Responsibilities

• Monitor sites and ensure study delivery per protocol.
• Prepare and maintain study documents and CTMS entries.
• Collaborate with LSAD and local study team for study execution.
• Ensure regulatory and quality requirements are met at sites.
• Assist in site training and monitoring visits (remote/on-site).
• Support data management and timely reporting of findings.

Skills

GCP/ICH knowledge

English communication

Entry-level CRA

Education

Science/healthcare degree

Job description

Thermo Fisher Scientific is seeking a Clinical Research Associate (CRA) to manage monitoring at allocated sites and collaborate with local study teams. You will ensure compliance with ICH-GCP, regulatory requirements, and study commitments, delivering high-quality data and site oversight.

Ideal candidates have 0-2 years of relevant experience, a degree in science/healthcare, and strong English communication skills.