Fortrea seeks a Senior Site Navigator to coordinate site-level activities during clinical trial start-up and closeout phases in Mexico City. The role involves serving as the primary liaison between sponsors, CROs, and investigative sites, managing regulatory compliance, site activation, and ongoing site support throughout the study lifecycle.
Responsibilities
Oversee site activation tasks aligned with ICH/GCP guidelines, local regulations, and project milestones
Identify prospective research sites, assess their capabilities, and conduct initial outreach and feasibility surveys
Collect, track, and review essential regulatory documents for site activation and ongoing compliance
Coordinate with study teams, vendors, and CRA staff to prepare for site initiation visits and manage study supplies




Liaise with IRBs, ethics committees, and regulatory authorities; manage contract negotiations and budget agreements with sites
Requirements
University degree in life sciences or allied health certification (nursing, medical, laboratory technology)
Minimum 3–5 years clinical research experience with ICH/GCP and regulatory knowledge
Alternative: High school diploma plus 5+ years clinical research experience
Fluent in local official language and English, written and verbal
Strong knowledge of ICH/GCP guidelines, regulatory affairs, and IRB/IEC regulations

📌 Senior Site Navigator (Xico)
🏢 Fortrea
📍 Xico