Junior Clinical Research Associate: Site Monitoring & Coordination

Fortrea; Buenos Aires; Vor Ort; ARS 64.569.000 - 98.390.000; Vollzeit

Zusammenfassung

Fortrea seeks a Site Monitor to manage clinical study sites, ensuring protocol adherence, data integrity, and timely reporting. The role involves on-site monitoring, initiation/closeout visits, and liaising with vendors under SOPs and regulatory guidelines.

The candidate should have a related degree and at least 6 months of experience, with proficiency in English and computer tools, and a valid driver's license for travel as required.

Qualifikationen

• Six months of experience in a related role (e.g., site monitoring, CRA, study coordinator).
• Basic understanding of regulatory guidelines (ICH GCP, ISO 14155 if applicable).
• Fluent in English; local office language proficiency as required.

Aufgaben

• Site monitoring and management of clinical study sites per SOPs and guidelines.
• Ensure informed consent and protocol adherence; verify data quality and CRF accuracy.
• Coordinate with sponsors/vendors, manage site budgets, and prepare trip reports.

Kenntnisse

Site monitoring

Study coordination

Regulatory knowledge

English proficiency

Project teamwork

Ausbildung

Bachelor's degree in a related field

Tools

CTMS

Microsoft Office

Jobbeschreibung

Fortrea seeks a Site Monitor to manage clinical study sites, ensuring protocol adherence, data integrity, and timely reporting. The role involves on-site monitoring, initiation/closeout visits, and liaising with vendors under SOPs and regulatory guidelines.

The candidate should have a related degree and at least 6 months of experience, with proficiency in English and computer tools, and a valid driver's license for travel as required.