Site Navigator Intern

Fortrea seeks a motivated intern to support clinical trial start-up and site management activities in Warsaw. The 12-month position offers hands-on exposure to the clinical trial lifecycle, including feasibility assessment, site activation, documentation management, and regulatory compliance within a global CRO environment.

Responsibilities

• Prepare, collect, review, and maintain study documentation and informed consent forms
• Support feasibility and site identification tasks including outreach and CDA collection
• Assist with Site Initiation Visit preparation and site activation activities
• Support document review, CRF review, and data validation upon training completion
• Coordinate study meetings and track payment workflows and invoices

Requirements

• Currently enrolled in or recently completed Master's in scientific, healthcare, or life sciences
• Strong organizational skills and meticulous attention to detail
• Fluent in Polish and English, written and verbal communication
• Interest in clinical research and drug development processes
• Ability to collaborate effectively within cross-functional teams
• Good Clinical Practice (GCP) knowledge preferred
• Prior internship, volunteer, or extracurricular experience valued