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.
Skills Required
- Degree in Life Sciences, Nursing, or a related field, or equivalent experience
- At least 6 months of independent clinical trial monitoring experience
- Understanding of clinical trial processes and regulatory requirements
- Strong organizational, communication, and problem-solving skills
- Fluency in English and local language skills
- Valid driver's license
- Willingness to travel to investigator sites
What We Do
Fortrea (Nasdaq: FTRE) is a leading global provider of clinical development and patient access solutions to the life sciences industry. We partner with emerging and large biopharmaceutical, medical device and diagnostic companies to drive healthcare innovation that accelerates life changing therapies to patients in need. Fortrea provides phase I-IV clinical trial management, clinical pharmacology, differentiated technology-enabled trial solutions and post-approval services. Fortrea’s solutions leverage three decades of experience spanning more than 20 therapeutic areas, a passion for scientific rigor, exceptional insights and a strong investigator site network. Our talented and diverse team working in more than 90 countries is scaled to deliver focused and agile solutions to customers globally. Learn more about how Fortrea is becoming a transformative force from pipeline to patient at Fortrea.com.
