Clinical Budget Builder (client-dedicated)
Full-timeMasters
Description
<p><span class="emphasis-2"><b>Join Our Team and Shape the Future of Clinical Research!</b></span></p><p></p><p>At <span class="emphasis-2"><b>Fortrea</b></span>, we are dedicated to streamlining clinical trials and ensuring compliance with global regulations. As a <span class="emphasis-2"><b>Site Budget Specialist</b>,</span> you will play a critical role in <span>the clinical trials budgeting process</span>. Your work will help drive the success of groundbreaking studies while ensuring compliance and efficiency.</p><p></p><p><span class="emphasis-2"><b>In this role, you will be part of our FSPx team and work directly with one of our renowned key sponsor to advance the development of innovative, life-changing medications.</b></span></p><p></p><p><span class="emphasis-2"><b>Key Responsibilities:</b></span></p><p>In this role, you will:</p><ul><li><p>Support Country Study site budget template, parameter, and payment term building to ensure timely setup of individual site budgets.</p></li><li><p>Manage and execute assigned study site budget maintenance activities through life of study.</p></li><li><p>Negotiate directly with globally assigned sites master clinical trial agreements rate cards.</p></li><li><p>Partner with site payment department to ensure site budget and payment terms compatibility with payment systems and EDC requirements.</p></li><li><p>Partner with internal Study Startup team, Clinical Operations teams, and TAU partners to improve overall SB&C metrics and implement processes.</p></li><li><p>Ensure standards are applied to the SB&C processes across projects, portfolios and support continuous improvement activities while developing TA-aligned strategies.</p></li><li><p>Leverage leading industry tools and data sources to provide budget and payment terms feedback aligned with parameters and fair market value guidance.</p></li><li><p>Promptly recognize and improve potential delays and escalate non-performance.</p><p></p></li></ul><p><span class="emphasis-2"><b>Required Qualifications:</b></span></p><p>To succeed in this role, you should have:</p><ul><li><p><b>Bachelor’s degree (LLB, JD, BA, or BS) preferred</b>; a university-level law degree is highly desirable (UK/EU).</p></li><li><p>Fortrea may consider <b>equivalent relevant experience</b> in lieu of educational requirements.</p></li><li><p><b>2–4 years of experience</b> in budget building, clinical research, or a related field.</p></li><li><p>Strong understanding of <b>ICH GCP guidelines</b> and clinical research processes.</p></li><li><p>Excellent <b>negotiation, communication, and organizational skills</b>.</p></li><li><p>Ability to work <b>independently and manage multiple priorities</b> in a fast-paced environment.</p></li><li><p>Proficiency in Microsoft Office and tracking systems.</p></li></ul><p></p><p><span class="emphasis-2"><b>What We Offer:</b></span></p><ul><li><p>Competitive salary and performance-based incentives.</p></li><li><p>Flexible work arrangements (remote/hybrid options).</p></li><li><p>Professional growth opportunities in a collaborative and innovative environment.</p></li><li><p>The opportunity to work on cutting-edge clinical research projects.</p></li></ul><p></p><p><span class="emphasis-2"><b>Ready to Make an Impact?</b></span></p><p>Take the next step in your career and join us in driving innovation in clinical research.</p><p></p><p><span class="emphasis-2"><b>Apply today!</b></span> Applications are reviewed on a rolling basis, don’t miss this opportunity!</p><p></p><p><span>Learn more about our </span><a href="https://careers.fortrea.com/us/en/eeo-and-accommodations" target="_blank">EEO & Accommodations request here</a><span>.</span></p>