CRA II: Site Monitoring & Study Start-Up

ThermoFisher Scientific; Comisión de Fomento de Perú; Hybrid; ARS 90,953,000 - 128,850,000; Full time

Job summary

Thermo Fisher Scientific in Argentina is seeking a Clinical Research Associate (CRA) to oversee delivery of studies at allocated sites and work with local study teams to ensure timely commitments. The CRA serves as main contact with sites, supervising monitoring visits and study conduct in line with ICH-GCP and AZ SOPs.

Experience level 0-2 years, English proficiency required; degree in scientific discipline.

Qualifications

• Good knowledge of clinical research regulatory requirements (GCP/ICH).
• Written and verbal English language skills.
• Ability to work with local study teams and investigators.

Responsibilities

• Contributes to site start-up, monitoring and regulatory maintenance.
• Trains, supports and advises investigators and site staff.
• Ensures study data quality and timely CTMS updates.
• Manages site visits (remote and on-site) and data checks.
• Ensures compliance with ICH-GCP and AZ SOPs.

Skills

Regulatory knowledge

GCP/ICH

English proficiency

Education

Scientific degree

Job description

Thermo Fisher Scientific in Argentina is seeking a Clinical Research Associate (CRA) to oversee delivery of studies at allocated sites and work with local study teams to ensure timely commitments. The CRA serves as main contact with sites, supervising monitoring visits and study conduct in line with ICH-GCP and AZ SOPs.

Experience level 0-2 years, English proficiency required; degree in scientific discipline.