Site Navigator Senior

Posted Yesterday
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Paris, Île-de-France, FRA
In-Office
Senior level
Biotech
The Role
Lead clinical trial site identification and start‑up activities, manage regulatory and ethics submissions, oversee site activation documentation, negotiate site contracts and budgets, perform remote Pre‑Study and in‑house CRA monitoring tasks, ensure TMF completeness and inspection readiness, and coordinate with CRAs and cross‑functional teams to meet timelines.
Summary Generated by Built In

Fortrea is looking for an experienced clinical operations professional to join our team as Senior Site Navigator, with a strong focus on clinical trial start‑up activities and in-house CRA responsibilities. This role is ideal for someone with solid start‑up expertise who is ready to take ownership of key processes within a global CRO environment.
 

Key Responsibilities

  • Manage site identification, feasibility, and full start‑up activities, including site outreach, feasibility questionnaires, and confidentiality agreements
  • Lead and coordinate Ethics Committee and Regulatory Authority submissions, including initial submissions and amendments
  • Drive and track essential regulatory documents to ensure timely and compliant site activation
  • Act as primary point of contact for investigative sites during start‑up and early study phases
  • Independently manage site contract and budget negotiations in collaboration with internal stakeholders
  • Perform remote Pre‑Study Visits and support Site Initiation Visit preparation
  • Conduct in‑house CRA activities such as document review, CRF review, data validation, and remote monitoring tasks
  • Ensure TMF completeness and inspection readiness
  • Collaborate closely with CRAs, project teams, and cross‑functional stakeholders to meet study timelines
     

Qualifications

  • University degree (life sciences preferred)
  • Minimum 3+ years of experience in Start‑Up
  • Strong hands-on experience in clinical trial start‑up is essential
  • Solid experience in contract and budget negotiations
  • Good knowledge of ICH/GCP and clinical trial processes

Learn more about our EEO & Accommodations request here.

Skills Required

  • University degree (life sciences preferred)
  • Minimum 3+ years of experience in Start-Up
  • Strong hands-on experience in clinical trial start-up
  • Solid experience in contract and budget negotiations
  • Good knowledge of ICH/GCP and clinical trial processes
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The Company
HQ: Durham, NC
10,811 Employees

What We Do

Fortrea (Nasdaq: FTRE) is a leading global provider of clinical development and patient access solutions to the life sciences industry. We partner with emerging and large biopharmaceutical, medical device and diagnostic companies to drive healthcare innovation that accelerates life changing therapies to patients in need. Fortrea provides phase I-IV clinical trial management, clinical pharmacology, differentiated technology-enabled trial solutions and post-approval services. Fortrea’s solutions leverage three decades of experience spanning more than 20 therapeutic areas, a passion for scientific rigor, exceptional insights and a strong investigator site network. Our talented and diverse team working in more than 90 countries is scaled to deliver focused and agile solutions to customers globally. Learn more about how Fortrea is becoming a transformative force from pipeline to patient at Fortrea.com.

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