Site Navigator - Site Readiness

Paris · On-site

About this 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.

Company at a glance

Fortrea (Nasdaq: FTRE) is a leading global clinical research organization (CRO) dedicated to providing innovative clinical development solutions to the life sciences industry. With over 30 years of clinical research experience, Fortrea has evolved from Covance and Labcorp into a pureplay CRO built for biotech, biopharma, medical device and diagnostic innovators.
Fortrea collaborates with both emerging and established companies to deliver agile, fit-for-purpose full service (FSO), functional service (FSP) and hybrid solutions. Fortrea provides comprehensive Phase I-IV clinical trial management, clinical pharmacology, and consulting services, backed by deep experience in more than 20 therapeutic areas.
Operating in approximately 100 countries, our diverse and talented team brings scientific rigor, operational excellence, and a strong investigator site network to every trial. By combining the best of our legacy experience with forward-thinking innovation, Fortrea brings predictability to clinical trial execution and helps transform aspirations into outcomes.
Together, exceptional is possible.
Learn more at Fortrea.com

Team Size10,001+ employees
WorkspaceOn-site
IndustryBiotechnology Research
Location
Paris, Ile-de-France, France
LinkedInLinkedIn

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