Clinical Research Associate II — Site Monitoring

ThermoFisher Scientific; Comisión de Fomento de Perú; Hybrid; ARS 55,000 - 85,000; Full time

Job summary

Thermo Fisher Scientific is seeking a Clinical Research Associate (CRA) to oversee delivery of clinical studies at allocated sites. You will monitor sites, ensure adherence to ICH-GCP and AZ SOPs, and collaborate with Local Study Teams to meet study commitments.

The role involves site initiation, monitoring visits (remote and on-site), data management collaboration, and timely reporting of study activities in CTMS, with potential for higher responsibilities based on tenure and performance.

Qualifications

• 0 - 2 years of prior relevant experience.
• Good knowledge of clinical research regulatory requirements (GCP/ICH).
• Written and verbal communication skills including good command of English.

Responsibilities

• Delivery of studies at allocated sites and monitoring according to plan.
• Coordinate with Local Study Team to ensure study commitments are met.
• Prepare, initiate, monitor and close sites per ICH-GCP and AZ SOPs.
• Ensure sites are inspection ready and provide feedback to Principal Investigator as required.
• Update CTMS and other systems with study data and timelines.

Education

Degree in scientific discipline or health care

Job description

Thermo Fisher Scientific is seeking a Clinical Research Associate (CRA) to oversee delivery of clinical studies at allocated sites. You will monitor sites, ensure adherence to ICH-GCP and AZ SOPs, and collaborate with Local Study Teams to meet study commitments.

The role involves site initiation, monitoring visits (remote and on-site), data management collaboration, and timely reporting of study activities in CTMS, with potential for higher responsibilities based on tenure and performance.