Senior Clinical Research Associate — Global Trials

Upsilon Global; Buenos Aires; On-site; ARS 1,200,000 - 1,800,000; Full time

Job summary

Upsilon Global is seeking a Senior Clinical Research Associate / CRA II to join their clinical operations team on a permanent basis in Argentina. The role involves monitoring sites across Argentina and internationally, ensuring ICH-GCP compliance, and collaborating with global study teams.

Travel within Argentina and occasional international travel are required. Ideal candidates have at least 2 years of CRA experience, strong monitoring skills, and fluency in Portuguese and English, with ability

Qualifications

• Minimum of 2 years' experience as a Clinical Research Associate.
• 2+ years clinical trial monitoring experience and independent monitoring visits.
• Experience with interventional trials and SDV/SDR.
• Strong knowledge of ICH-GCP and regulatory requirements.
• Experience across the full study lifecycle and site management.

Responsibilities

• Conduct Site Selection, Site Initiation, Monitoring and Close-Out visits.
• Monitor sites per protocol, sponsor requirements and regulations.
• Perform SDV/SDR and ensure data quality and patient safety.
• Review informed consent and manage protocol deviations and risks.
• Provide guidance to investigators and maintain robust site communications.
• Prepare monitoring reports and ensure inspection-ready documentation.
• Support study start-up, recruitment, maintenance and close-out activities.

Skills

Site monitoring

Independent monitoring visits

SDV / SDR

Regulatory compliance

ICH-GCP knowledge

Study lifecycle experience

Site issue resolution

Communication with sites

Travel readiness

Team collaboration

Tools

Veeva

Oracle

Medidata RAVE

CTMS

eTMF systems

MS Word

MS Excel

MS PowerPoint

MS Project

Job description

Upsilon Global is seeking a Senior Clinical Research Associate / CRA II to join their clinical operations team on a permanent basis in Argentina. The role involves monitoring sites across Argentina and internationally, ensuring ICH-GCP compliance, and collaborating with global study teams.

Travel within Argentina and occasional international travel are required. Ideal candidates have at least 2 years of CRA experience, strong monitoring skills, and fluency in Portuguese and English, with ability