Clinical Research Associate I: Drive Impact in Trials

ThermoFisher Scientific; Buenos Aires; On-site; ARS 1,200,000 - 1,800,000; Full time

Job summary

Thermo Fisher Scientific is seeking a Clinical Research Associate I to join our global trials team in Argentina. You will monitor investigator sites, ensure protocol and regulatory adherence, and support site management and documentation across multiple studies.

You will coordinate monitoring activities remotely or on-site, maintain essential documents, and contribute to trial readiness while collaborating with sponsors, sites, and internal teams to ensure data integrity and patient safety.

Qualifications

• Bachelor’s degree in a life sciences field or RN, with relevant clinical research training.
• Minimal clinical monitoring experience in trials or healthcare environments.
• Valid driver's license where applicable.

Responsibilities

• Monitor investigator sites using risk-based approaches and ensure data accuracy.
• Coordinate site qualification, initiation, and close-out activities.
• Prepare essential documents per ICH-GCP and regulatory requirements.
• Provide status updates and maintain study systems and documentation.
• Communicate with sites, client teams, and regulatory bodies as needed.

Skills

Clinical monitoring

ICH-GCP knowledge

Regulatory compliance

Site management

Documentation quality

Communication skills

Problem solving

Team collaboration

Education

Bachelor's degree in life sciences or RN

Tools

Microsoft Office

Job description

Thermo Fisher Scientific is seeking a Clinical Research Associate I to join our global trials team in Argentina. You will monitor investigator sites, ensure protocol and regulatory adherence, and support site management and documentation across multiple studies.

You will coordinate monitoring activities remotely or on-site, maintain essential documents, and contribute to trial readiness while collaborating with sponsors, sites, and internal teams to ensure data integrity and patient safety.