Oncology CRA I — Global Trials & Monitoring

KCR Placement; Buenos Aires; On-site; ARS 69,181,000 - 92,241,000; Full time

Job summary

ICON Strategic Solutions in Buenos Aires is seeking a Clinical Research Associate I to join our sponsor-dedicated team. You will contribute to clinical trial monitoring across programmes, ensuring high-quality outcomes in a collaborative environment.

You will manage site coordination, queries, and study documentation, while maintaining patient safety and regulatory compliance. Travel up to approximately 45% and fluent English are required.

Qualifications

• Clinical trial monitoring experience required.
• Knowledge of ICH-GCP guidelines and ability to review medical data.
• Oncology protocol experience.
• Excellent written and verbal English communication.
• Willingness to travel approximately 45%.
• Based in Buenos Aires.

Responsibilities

• Deliver clinical trial monitoring to a high standard.
• Coordinate activities for setting up and monitoring a study and maintain study documentation.
• Run sponsor-generated queries and support study cost efficiency.
• Develop and maintain strong relationships with stakeholders, investigators, and site staff.
• Ensure patient safety by complying with ICON's procedures, protocols, and regulatory requirements.

Skills

ICH-GCP guidelines knowledge

English communication

Oncology protocol experience

Travel willingness (45%)

Based in Buenos Aires

Education

University degree in medicine, science, or equivalent

Job description

ICON Strategic Solutions in Buenos Aires is seeking a Clinical Research Associate I to join our sponsor-dedicated team. You will contribute to clinical trial monitoring across programmes, ensuring high-quality outcomes in a collaborative environment.

You will manage site coordination, queries, and study documentation, while maintaining patient safety and regulatory compliance. Travel up to approximately 45% and fluent English are required.