Clinical Research Associate II - FSO

<p><b>Be the connection between science and solutions.</b><span><span> </span>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.</span> This role will offer you the opportunity to <span>directly influence the success of global clinical trials and the delivery of innovative therapies to patients worldwide. </span></p><p></p><p><span class="emphasis-2"><b><i>This role is for upcoming future opportunities that may arise at Fortrea</i></b></span></p><p></p><p><b><span class="emphasis-2">Key Responsibilities:</span></b></p><ul><li><p>Manage clinical trial sites in alignment with Fortrea SOPs, ICH-GCP, project plans, and sponsor requirements, including oversight of training documentation and regulatory compliance.</p></li><li><p>Conduct all phases of site monitoring visits (pre-study, initiation, routine, and close-out), ensuring subject safety, protocol adherence, and data integrity.</p></li><li><p>Perform source data verification, query resolution, and eCRF review to ensure high-quality, audit-ready clinical data.</p></li><li><p>Maintain and update essential documents in eTMF and sponsor systems, ensuring regulatory and documentation completeness throughout the study lifecycle.</p></li><li><p>Monitor investigational product (IP) accountability, storage, and compliance with protocol and regulatory standards.</p></li><li><p>Collaborate with cross-functional teams to align site performance with study timelines, metrics, and quality expectations.</p></li></ul><p></p><p><b><span class="emphasis-2">Required Qualifications :</span></b></p><ul><li><p>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.</p></li><li><p>Solid understanding of ICH-GCP guidelines and local regulatory requirements governing clinical research.</p></li><li><p>Working knowledge of clinical trial processes and monitoring procedures.</p></li><li><p>Strong attention to detail and ability to follow complex protocols and documentation standards.</p></li><li><p>Fluent in English both written and verbal.</p></li><li><p>Proficient in using clinical systems and tools; able to work independently and travel as required.</p></li></ul><p></p><p><b><span class="emphasis-2">Why Join Us? </span></b></p><ul><li><p>Contribute to advancing innovative therapies and improving patient outcomes through meaningful clinical research on a global scale.</p></li><li><p>Thrive in a collaborative environment that values continuous learning, mentorship, and professional development.</p></li><li><p>Work with modern clinical technologies and streamlined systems that support efficiency, quality, and compliance.</p></li><li><p>Benefit from a flexible work model, competitive benefits, and a strong commitment to employee well-being.</p></li></ul><p></p><p><span>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. </span><span>If you are seeking a rewarding opportunity within a globally respected organization, we encourage you to submit your application today.</span></p><p></p><p></p><p></p><p><span>Learn more about our </span><a href="https://careers.fortrea.com/us/en/eeo-and-accommodations" target="_blank">EEO &amp; Accommodations request here</a><span>.</span></p>