Site Navigator I

**Site Navigator I** **Location: remote**   We are looking for a **clinical operations professional** to join our team as **Site Navigator I**, managing clinical trial **start‑up activities** with additional **in‑house CRA responsibilities**. This is an excellent, comprehensive role for someone looking to grow their career in clinical research within a global CRO environment. **Key Responsibilities** * Perform **site identification, feasibility, and start‑up activities**, including site outreach, feasibility questionnaires, and confidentiality agreements * Coordinate and track **essential regulatory documents** to ensure timely and compliant site activation * Act as a **primary point of contact for investigative sites** during the start‑up and possibly the maintenance phase * Perform **ethics committee and regulatory authority submissions**, renewals, and prepare the relevant regulatory documentation in collaboration with internal teams * Perform **site contract and budget negotiations** under guidance * Perform **remote Pre-Study Visits** * Support **Site Initiation Visit (SIV) preparation**, including coordination of documents, systems access, and study supplies * Perform **remote/in‑house CRA activities**, such as document review, CRF review, data validation, and remote monitoring tasks (after required training) * Maintain accurate documentation in study systems and ensure the **TMF is inspection‑ready** * Collaborate closely with CRAs, project teams, and study stakeholders to support study milestones **Qualifications** * University degree (life sciences preferred) * Minimum 1 year experience in Clinical Operations or Start-Up * Knowledge of **ICH/GCP** and clinical trial processes * Strong organizational skills, attention to detail, effective communication and willingness to learn * Ability to manage multiple tasks in a structured and proactive way Learn more about our [EEO & Accommodations request here](https://careers.fortrea.com/us/en/eeo-and-accommodations).