Clinical Research Associate I: Site Monitor

Fortrea; Tandil; On-site; ARS 76,867,000 - 138,361,000; Full time

Job summary

Fortrea is seeking a Site Monitor to oversee clinical studies in Argentina, ensuring adherence to SOPs, regulatory guidelines, and project plans. You will monitor sites, manage data integrity, and support site staff through monitoring visits.

The role requires regulatory knowledge, English fluency, and the ability to work in a matrix environment, with travel as needed to sites and sites, and driving license preferred.

Qualifications

• Degree or certification in a related allied health field.
• Fluent in English, both written and spoken.
• Basic knowledge of Regulatory Guidelines.
• Basic understanding of the clinical trial process.

Responsibilities

• Site monitoring including routine monitoring and closeout of clinical sites.
• Monitor data integrity through source document review.
• Prepare accurate and timely trip reports.
• Interact with internal teams to evaluate needs and timelines.
• Assist with training and development of new staff.
• Coordinate designated clinical projects as Local Project Coordinator (with supervision).
• Perform other duties as assigned by management.

Skills

Fluent English

Regulatory guidelines

Clinical trial process

CTMS experience

Driver's License

Team collaboration

Education

University degree

Allied health certification

Job description

Fortrea is seeking a Site Monitor to oversee clinical studies in Argentina, ensuring adherence to SOPs, regulatory guidelines, and project plans. You will monitor sites, manage data integrity, and support site staff through monitoring visits.

The role requires regulatory knowledge, English fluency, and the ability to work in a matrix environment, with travel as needed to sites and sites, and driving license preferred.