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.
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 monitori...
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.
View more
View less