Cra 2 - Sponsor Dedicated

We are hiring an experienced **CRA II** to join our **sponsor‑dedicated team in Poland**. In this role, you’ll work exclusively with one sponsor, gaining deep study knowledge and long‑term project ownership, with strong opportunities for career growth.   ---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------- ### Key Responsibilities * Perform site monitoring activities (initiation, routine monitoring, and close‑out visits) * Manage clinical sites in line with project plans, SOPs, and regulatory requirements * Ensure patient safety, data quality, and audit readiness * Review CRFs, perform source data verification, and resolve queries * Track and follow up on **Serious Adverse Events (SAEs)** * Prepare accurate monitoring and trip reports * Support feasibility, QC visits, investigator recruitment, and regulatory submissions * Collaborate with sponsors, investigators, and internal teams * Support training and mentoring of new team members   ### Requirements * University degree in **Life Sciences** or **Nursing** * **Minimum 2 years** of independent monitoring experience in Pharma/CRO * Experience in **interventional studies** * Strong knowledge of **SAE reporting** * Oncology experience is a plus (or willingness to work in Oncology) * **Fluent English and Polish**   ### Why join? * Dedicated to **one sponsor** * Exposure to complex, international studies * Clear **career progression** * Supportive and collaborative team environment Learn more about our [EEO & Accommodations request here](https://careers.fortrea.com/us/en/eeo-and-accommodations).