Clinical Research Associate I: Site Monitoring & Study Coordination

FTARG Fortrea Argentina S.A.; Buenos Aires; Vor Ort; ARS 900.000 - 1.300.000; Vollzeit

Zusammenfassung

Fortrea Argentina S.A. is seeking a Clinical Site Monitor to oversee site management and monitoring of clinical studies in accordance with SOPs and regulatory guidelines.

The role involves coordinating visits, CRF review, vendor liaison, and training of staff, with travel as required, ensuring data integrity and audit readiness.

Candidates should have a university degree, English fluency, and at least 6 months of relevant experience; on-site work in Buenos Aires area.

Qualifikationen

• University degree or allied health certification from an accredited institution.
• Six months of experience in site management, CRA, or related roles.
• Fluency in English; local language required.
• Understanding of Regulatory Guidelines and ICH-GCP.
• Ability to work in a matrix environment and to travel as needed.

Aufgaben

• Monitor and manage study sites including initiation visits and closeout.
• Ensure informed consent and protocol adherence; maintain study files.
• Review CRFs to ensure data integrity and resolve data issues.
• Liaise with vendors and coordinate trial logistics.
• Prepare accurate trip reports and ensure audit readiness.
• Support training and mentoring of new staff.

Kenntnisse

Clinical monitoring

Team collaboration

Problem solving

English proficiency

Ausbildung

University degree or allied health certification

Tools

CTMS

Microsoft Office

Jobbeschreibung

Fortrea Argentina S.A. is seeking a Clinical Site Monitor to oversee site management and monitoring of clinical studies in accordance with SOPs and regulatory guidelines.

The role involves coordinating visits, CRF review, vendor liaison, and training of staff, with travel as required, ensuring data integrity and audit readiness.

Candidates should have a university degree, English fluency, and at least 6 months of relevant experience; on-site work in Buenos Aires area.