Description
The Clinical Research Budgets Specialist will develop, review, and negotiate site-level clinical trial budgets and contract payment terms for U.S. and international research sites. The role interprets study protocols and evolving requirements, ensures all site costs are captured, manages budget amendments, coordinates with sponsors and CROs, supports Clinical Trial Agreement alignment, maintains audit-ready records, and builds scalable processes. The position requires a bachelor's degree or equivalent experience and at least two years of site-side clinical research budgeting or trial finance experience, with international, CTMS, VAT, and billing-compliance experience preferred. It offers a hybrid work arrangement with in-office collaboration two days per week in New York City, Cambridge, or Southlake, plus medical, dental, vision, retirement, wellness, and other benefits.
