Unblinded CRA I

Fortrea

Job Location:

Maidenhead - UK

Monthly Salary: Not Disclosed

Posted on: Yesterday

Vacancies: 1 Vacancy

Job Summary

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 youll 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 were 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 drivers 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.

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 youll do:Monitor and m...