Site Navigator

Site Navigator II

Location: Türkiye (Home‑Based or Office-based in Istanbul)

About the Role

The Site Navigator II supports the start‑up and activation of clinical trial sites in Türkiye.

Acting as the main point of contact for investigative sites, you ensure timely site activation, regulatory compliance, and effective collaboration between sites, sponsors, and Fortrea study teams.

Key Responsibilities

• Coordinate site‑level start‑up activities in line with ICH‑GCP, local regulations, SOPs, and study requirements
• Identify and assess potential sites; conduct initial outreach and feasibility activities
• Support remote pre‑study visits and site selection documentation
• Collect, review, and track essential regulatory documents for site activation and maintenance
• Support submissions to IRB/IEC and Regulatory Authorities in collaboration with internal teams
• Maintain ongoing site regulatory compliance (renewals, document tracking, investigator changes)
• Support ICF review, customization, and local requirements
• Serve as the primary contact for investigative sites and support CRA teams during site initiation
• Ensure accurate TMF filing and continuous audit readiness
• Participate in project meetings and escalate site‑level risks or issues as needed

Qualifications

• Degree in Life Sciences or related field, or equivalent clinical research experience
• 2+ years of experience in clinical research, study start‑up, or regulatory processes
• Solid knowledge of ICH‑GCP and local regulatory requirements
• Strong organizational and communication skills
• Fluent in Turkish and English

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