Fortrea is looking for a CRA I to join our multisponsor team in Central Poland, with a preference for candidates based in or near Warsaw. This is an exciting opportunity to gain exposure to a variety of clinical studies while growing your monitoring career within a global CRO.
 

What you'll do

• Perform on-site and remote monitoring visits in line with study protocols, ICH-GCP, and regulatory requirements.
• Support sites from study start-up through close-out.
• Review source data and ensure data quality and patient safety.
• Build strong relationships with investigators and site staff.
• Track study progress and prepare monitoring reports.
• Support audit and inspection readiness.
   

What we're looking for

• Life science degree, nursing qualification, or equivalent scientific background.
• At least 6 months to 1 year of independent site monitoring experience as a CRA.
• Experience in interventional clinical trials.
• Good understanding of ICH-GCP and clinical trial processes.
• Strong communication, organizational, and problem-solving skills.
• Fluent in Polish and English.
• Willingness to travel within Poland.
   

Why Fortrea?

• Join a supportive and collaborative team.
• Work across a variety of therapeutic areas and studies.
• Gain valuable experience in a multisponsor environment.
• Access clear career development opportunities and ongoing training.
• Be part of a global organization helping bring innovative treatments to patients.
   

Interested? Apply today and continue building your CRA career with Fortrea.