Junior Clinical Research Associate - Site Monitoring

NoxPharm; Tandil; On-site; ARS 92,241,000 - 138,361,000; Full time

Job summary

Fortrea is seeking a Site Monitoring Specialist to oversee clinical study sites and manage site activities. You will ensure proper initiation, conduct visits, and maintain study files while safeguarding patient safety and data integrity.

The role requires coordination with sponsors, adherence to SOPs, and efficient travel; English fluency and regulatory knowledge are essential. A relevant degree and at least six months in a related role are expected.

Qualifications

• University degree or certification in a related allied health field; equivalent experience considered.
• Fluent English and local language, both written and verbal.
• Basic understanding of regulatory guidelines and clinical trial process.
• Minimum 6 months in site management, CRA, or related role.
• Valid driver's license required.

Responsibilities

• Monitor and manage clinical sites, conduct visits, and maintain study files.
• Ensure informed consent and protocol adherence per regulatory requirements.
• Review data for accuracy and integrity; manage SAEs and reporting.
• Coordinate travel and site resources efficiently; support budget tracking.
• Prepare trip reports and liaise with vendors and internal teams.

Skills

Regulatory knowledge

English proficiency

Team collaboration

Planning and organization

Problem solving

Communication

Valid driver’s license

Education

University degree or allied health certification

Tools

CTMS

MS Office

Job description

Fortrea is seeking a Site Monitoring Specialist to oversee clinical study sites and manage site activities. You will ensure proper initiation, conduct visits, and maintain study files while safeguarding patient safety and data integrity.

The role requires coordination with sponsors, adherence to SOPs, and efficient travel; English fluency and regulatory knowledge are essential. A relevant degree and at least six months in a related role are expected.