Be the connection between science and solutions. In this CRA position, you’ll help transform complex clinical protocols into real-world results, working alongside a team that values precision, integrity, and progress. This role will offer you the opportunity to directly influence the success of global clinical trials and the delivery of innovative therapies to patients worldwide.
This role is for upcoming future opportunities that may arise at Fortrea
Key Responsibilities:
Manage clinical trial sites in alignment with Fortrea SOPs, ICH-GCP, project plans, and sponsor requirements, including oversight of training documentation and regulatory compliance.
Conduct all phases of site monitoring visits (pre-study, initiation, routine, and close-out), ensuring subject safety, protocol adherence, and data integrity.
Perform source data verification, query resolution, and eCRF review to ensure high-quality, audit-ready clinical data.
Maintain and update essential documents in eTMF and sponsor systems, ensuring regulatory and documentation completeness throughout the study lifecycle.
Monitor investigational product (IP) accountability, storage, and compliance with protocol and regulatory standards.
Collaborate with cross-functional teams to align site performance with study timelines, metrics, and quality expectations.
Required Qualifications :
University or college degree in life sciences, nursing, pharmacy, or a related allied health profession; equivalent relevant experience may be considered in lieu of formal education.
Solid understanding of ICH-GCP guidelines and local regulatory requirements governing clinical research.
Working knowledge of clinical trial processes and monitoring procedures.
Strong attention to detail and ability to follow complex protocols and documentation standards.
Fluent in English both written and verbal.
Proficient in using clinical systems and tools; able to work independently and travel as required.
Why Join Us?
Contribute to advancing innovative therapies and improving patient outcomes through meaningful clinical research on a global scale.
Thrive in a collaborative environment that values continuous learning, mentorship, and professional development.
Work with modern clinical technologies and streamlined systems that support efficiency, quality, and compliance.
Benefit from a flexible work model, competitive benefits, and a strong commitment to employee well-being.
We invite qualified candidates who are committed to excellence in clinical research to apply and become part of Fortrea’s mission to advance healthcare worldwide. If you are seeking a rewarding opportunity within a globally respected organization, we encourage you to submit your application today.
Learn more about our EEO & Accommodations request here.
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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.
