CRA II: Clinical Site Monitor & Regulatory Expert

ThermoFisher Scientific; Chile; Remote; CLP 11,160,000 - 20,088,000; Full time

Job summary

Thermo Fisher Scientific is seeking a Clinical Research Associate (CRA) to oversee local study sites in Chile, ensuring study conduct meets ICH-GCP and AZ SOPs. You will act as the main contact, coordinate site activities, and support study teams across monitoring visits and regulatory tasks.

With 0-2 years of relevant experience and strong communication skills, you will monitor sites, assist with start-up and closure, and contribute to data quality and safety reporting.

Qualifications

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

Responsibilities

• Monitor study sites and ensure delivery per protocol and timelines.
• Prepare, initiation, monitoring and closure of sites in line with AZ SOP and ICH-GCP.
• Train, support and advise investigators and site staff on study activities.

Skills

Regulatory knowledge

Communication skills (English)

Education

Science/healthcare degree

Job description

Thermo Fisher Scientific is seeking a Clinical Research Associate (CRA) to oversee local study sites in Chile, ensuring study conduct meets ICH-GCP and AZ SOPs. You will act as the main contact, coordinate site activities, and support study teams across monitoring visits and regulatory tasks.

With 0-2 years of relevant experience and strong communication skills, you will monitor sites, assist with start-up and closure, and contribute to data quality and safety reporting.