Skip to content
← Back to job listings

Site Navigator - Site Readiness

FTFRA Fortrea France SARL · Remote, France

Entry LevelRemoteExternal listingfull-time7 days ago

About The Role

  • Ready to take the next step in your clinical research career?
  • We are seeking a motivated Clinical Operations professional to join our team as a Site Navigator I.
  • This role offers the opportunity to gain valuable experience, collaborate with
  • global teams, and grow within a leading CRO.

Summary of Responsibilities

  • Act as the primary point of contact for investigative sites throughout the course of the study
  • Conduct site outreach, feasibility and perform remote Pre-Study Visits
  • Collect, track, and perform a quality review of all essential documents required for the site activation and for the maintenance of site regulatory compliance throughout the study
  • Support the CRA team in preparing for Site Initiation Visits to ensure timely distribution of clinical study supplies, accesses, and documents
  • Perform remote visits as required by the monitoring plan
  • Perform Case Review Form (CRF) review and monitoring of site protocol deviations and Serious Adverse Event (SAE) reporting
  • Actively participate in study team meetings to support study progress, develop, and implement action plans for site level risks, underperforming sites, or issues impacting project milestones and escalate issues in a timely manner
  • Maintain accurate documentation in study systems and ensure the TMF is inspection‑ready
  • Perform country and site Participant Information Sheets/Informed Consent Forms review/customization as applicable
  • Manage country and site level documents for Part II submission under EU CTR or for Ethics Committees, Third Bodies and Regulatory Authorities as applicable
  • Perform site contracts and budget negotiations as applicable

Qualifications (Minimum Required)

  • University degree (life sciences preferred)
  • 1-2 years’ experience in Clinical Operations and/or Start-Up
  • Knowledge of ICH/GCP, EU CTR and clinical trial processes/regulations
  • Effective communication
  • Fluent in English and French (written and spoken)
  • Organizational skills, attention to detail, and willingness to learn
  • Ability to manage multiple tasks in a structured and proactive way

Learn more about our EEO & Accommodations request here .

This is an external listing. JobSpring does not represent or verify the employer. Report this listing