Clinical Research Associate I: Impactful Trials

ThermoFisher Scientific; Buenos Aires; On-site; ARS 600,000 - 1,200,000; Full time

Job summary

Thermo Fisher Scientific is seeking a Clinical Research Associate I to support monitoring and site management across trials, ensuring protocol and regulatory compliance.

You will conduct remote or on-site visits, manage essential documents per ICH-GCP guidelines, and collaborate with sponsors and investigational sites to guarantee patient safety and data integrity. The role emphasizes timely reporting and proactive issue resolution.

Qualifications

• Bachelor's degree in life sciences or RN certification required.
• Minimal clinical monitoring experience or relevant clinical/trials healthcare experience considered.
• Valid driver's license where applicable.
• Equivalency may be considered with education, training, or related experience.

Responsibilities

• Monitor investigator sites with a risk-based monitoring approach and ensure data accuracy through SDR/SDV/CRF review.
• Assess investigational product through inventory and records review; document observations in reports.
• Escalate deficiencies and ensure issues are resolved with clinical management.
• Participate in investigator meetings; help identify qualified investigators with the client.
• Ensure essential documents are complete according to ICH-GCP and regulations.
• Provide trial status updates and keep study systems current; support regulatory audits/inspections.

Skills

ICH GCP knowledge

Communication skills

Interpersonal skills

Time management

MS Office

English language

Critical thinking

Teamwork

Problem solving

Risk-based monitoring

Education

Bachelor's degree in life sciences / RN

Job description

Thermo Fisher Scientific is seeking a Clinical Research Associate I to support monitoring and site management across trials, ensuring protocol and regulatory compliance.

You will conduct remote or on-site visits, manage essential documents per ICH-GCP guidelines, and collaborate with sponsors and investigational sites to guarantee patient safety and data integrity. The role emphasizes timely reporting and proactive issue resolution.