Junior Clinical Research Monitor: Transform Global Trials

Fortrea; Warszawa; On-site; PLN 120,000 - 200,000; Full time

Job summary

Fortrea is seeking a Clinical Research Associate to oversee site monitoring for multicenter trials in line with ICH GCP and Fortrea SOPs. You will verify training records, perform 100% source data verification, and ensure regulatory documents are complete.

Travel up to 60% is required; the role emphasizes data integrity, site initiation, and ongoing collaboration with sponsors and study teams in a fast-paced, global environment.

Qualifications

• University or college degree in a related allied health field or nursing licensure.
• Thorough knowledge of ICH GCP and local regulatory requirements.
• Fluent in the local language and in English, both written and verbal.

Responsibilities

• Manage clinical trial sites according to SOPs and GCP.
• Perform monitoring visits including pre-study, initiation, routine, and close-out.
• Ensure data integrity and regulatory document completeness.
• Assist with training of site staff and monitoring plan development.

Skills

Clinical Monitoring

ICH GCP

Site Management

English

Travel

Education

Bachelor's degree in life sciences

Tools

eClinical systems

eTMF

Job description

Fortrea is seeking a Clinical Research Associate to oversee site monitoring for multicenter trials in line with ICH GCP and Fortrea SOPs. You will verify training records, perform 100% source data verification, and ensure regulatory documents are complete.

Travel up to 60% is required; the role emphasizes data integrity, site initiation, and ongoing collaboration with sponsors and study teams in a fast-paced, global environment.