Join Fortrea and play a key role in advancing clinical research while ensuring the highest standards of patient safety and data quality. This is a client-dedicated Unblinded CRA I role, supporting clinical trials where access to treatment assignment information is required.
 

What you'll do:

• Monitor and manage clinical trial sites from start-up through closeout.
• Conduct site visits, training, and ongoing support for study teams.
• Ensure compliance with study protocols, ICH-GCP guidelines, and regulatory requirements.
• Review source data and documentation to ensure accuracy and quality.
• Support audit readiness and issue resolution at site level.
• Collaborate with sponsors, vendors, and cross-functional teams to keep studies on track.
• Travel to investigator sites as required.
   

What we're looking for:

• Degree in Life Sciences, Nursing, or a related field (or equivalent experience).
• At least 6 months of independent monitoring experience.
• Understanding of clinical trial processes and regulatory requirements.
• Strong organizational, communication, and problem-solving skills.
• Fluent English and local language skills.
• Valid driver's license and willingness to travel.
   

This is a great opportunity to develop your CRA career while contributing to clinical studies that make a difference to patients worldwide!

Learn more about our EEO & Accommodations request here.