Job Description

Fortrea is currently recruiting a CRA II to join our multisponsor team in Poland on a permanent, full-time contract

This is a unique opportunity for a CRA based in Poland to support clinical trial monitoring in the UK and Ireland The role may involve regular travel abroad to conduct on-site monitoring activities. The duration and frequency of international travel may vary depending on project needs, so we are looking for candidates open and willing to travel internationally when required

The successful candidate will be employed in Poland under a Polish employment contract and local compensation structure, while contributing to international clinical trials and gaining valuable exposure to sites in the UK and Ireland

Key Responsibilities

• Perform all aspects of site monitoring including site initiation, routine monitoring, and close-out visits

• Ensure protocol compliance, GCP adherence, and patient safety

• Conduct source data verification and CRF review

• Identify and follow up on missing or inconsistent data

• Maintain site documentation and study files

• Support site management and investigator communication

• Ensure audit readiness at site level

• Prepare accurate and timely monitoring reports

• Track and follow up on Serious Adverse Event (SAE) reporting

• Participate in feasibility activities and site identification

• Support training activities and co-monitoring when required

• May act as a local project contact for designated studies
  

Education & Qualifications

• University degree in life sciences, nursing, or a related field

• Minimum 2 years of independent monitoring experience in an international Pharma/CRO environment

• Experience in interventional clinical trials

• Oncology experience preferred, or willingness to work on oncology studies

• Strong understanding of SAE reporting

• Fluent in English and Polish

• Willingness to travel internationally to the UK and Ireland

Learn more about our EEO & Accommodations request here