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