CRA I: Clinical Trial Monitoring & Coordination

ICON; Buenos Aires; Presencial; ARS 63.383.000 - 98.092.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Annual leave entitlements

Health insurance

Retirement planning

LifeWorks EAP

Descripción de la vacante

ICON Strategic Solutions is seeking a Clinical Research Associate I to contribute to our sponsor-dedicated clinical trial operations. You will deliver monitoring activities and help ensure high-quality data across programmes within ICON's global framework.

You will coordinate site activities, manage sponsor queries, and support cost efficiency while maintaining strong relationships with investigators and site staff. Travel up to 35% is expected.

Formación

• University degree in medicine, science, or equivalent.
• Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data.
• Excellent written and verbal communication in English.
• Willingness to travel approximately 35%.

Responsabilidades

• Deliver clinical trial monitoring work to a high standard and coordinate study activities.
• Coordinate sponsor-generated queries and contribute to study cost efficiency.
• Develop strong relationships with investigators and site staff.
• Ensure patient safety by adhering to ICON procedures and regulatory requirements.

Conocimientos

ICH-GCP guidelines knowledge

Clinical trial monitoring

Excellent communication (English)

Educación

University degree in medicine/science

Descripción del empleo

ICON Strategic Solutions is seeking a Clinical Research Associate I to contribute to our sponsor-dedicated clinical trial operations. You will deliver monitoring activities and help ensure high-quality data across programmes within ICON's global framework.

You will coordinate site activities, manage sponsor queries, and support cost efficiency while maintaining strong relationships with investigators and site staff. Travel up to 35% is expected.