other
Posted May 7Site Navigator I
at Fortrea
Warsaw, PolandHybrid
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 occasionally the maintenance phase Perform ethics committee and regulatory authority/EU CTR submissions , renewals, and prepare the relevant regulatory
Requirements
- Qualifications (Minimum Required): University degree (life sciences preferred) Minimum 1 year
- experience in Clinical Operations or Start-Up Knowledge of ICH/GCP and clinical trial processes Fluent Polish and English (written and spoken) 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 .
Additional details
- Job Overview: Location: Warsaw (hybrid role) 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. Summary of