Senior Research Budget Specialist - Cardiology

Iterative Health

• $95K — $115K *
Healthcare
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree or equivalent experience.
  • 4-6 years of site-side clinical research budgeting experience with a focus on complex negotiations.
  • Deep understanding of site-level clinical trial operations across diverse geographies.
  • Proven ability to independently lead complex budget negotiations with sponsors and CROs.
  • Strong judgment in ambiguous situations, capable of assessing risk and driving issues to resolution.
  • Excellent communication and stakeholder management skills.
  • Ability to handle a high-volume workload across multiple priorities.

Responsibilities

  • Lead development and negotiation of site-level clinical trial budgets for high-value studies.
  • Serve as an expert on complex budget scenarios involving multi-country studies and novel payment structures.
  • Construct accurate and competitive site budgets based on study protocols and requirements.
  • Proactively identify budget gaps and resolve issues with internal and external stakeholders.
  • Ensure all site costs are captured in budgets, including patient procedures and administrative fees.
  • Review and manage budget amendments as studies evolve.
  • Account for region-specific factors such as currency and local payment practices.

Benefits

  • Hybrid work environment with required in-office days for collaboration.
  • Comprehensive health coverage with up to 80% premium coverage.
  • Mental health support services provided.
  • Unlimited PTO plus 12 company holidays and an annual shutdown.
  • 401(k) plan with company match up to 3%.
  • Weekly in-office lunch benefit.
  • 100% company-paid short and long-term disability coverage.
Full Job Description
The Senior Clinical Research Budgets Specialist is a seasoned, strategic partner to the sites within Iterative Health's growing domestic and international network - taking ownership of the most complex, high-value clinical trial budget negotiations and contract payment terms across the portfolio. This role demands a deep understanding of site-level trial operations, sharp negotiation instincts, and the ability to navigate sophisticated sponsor and CRO relationships across multiple geographies. The ideal candidate brings 4-6 years of hands-on clinical research budgeting experience, a track record of independently resolving complex financial and contractual challenges, and the judgment to operate with confidence where precedent is limited and the stakes are high.

Where You'll Drive Impact
  • Lead development, review, and negotiation of site-level clinical trial budgets and payment terms for high-value and complex studies across U.S. and international research sites.
  • Serve as the internal expert on complex budget scenarios - including multi-country studies, novel endpoints, investigational devices, and non-standard sponsor payment structures.
  • Interpret sophisticated study protocols, schedules of assessments, and evolving study requirements to construct accurate, defensible, and competitive site budgets.
  • Proactively identify gaps, inconsistencies, or underrepresented cost considerations and drive resolution with sponsors, CROs, and internal stakeholders.
  • Ensure budgets appropriately capture all site costs including per-patient procedures, startup activities, administrative fees, and pass-through expenses.
  • Review and manage budget and payment amendments as studies evolve, including escalated or disputed items.
  • Account for country-specific considerations such as currency, tax/VAT, payment cadence, and local site practices across geographies.
  • Serve as a senior point of contact for sponsor and CRO budget discussions on complex or high-priority studies.
  • Support alignment between Clinical Trial Agreements (CTAs) and negotiated budget and payment terms.
  • Navigate sponsor pushback, non-standard terms, and escalated disputes with confidence and professionalism.
  • Maintain clear documentation and audit-ready records throughout the budget lifecycle.
  • Collaborate with site leadership, research coordinators, regulatory teams, and finance partners to support timely study start-up across competing priorities.
  • Contribute to the development of scalable budgeting tools, templates, and processes that improve consistency and efficiency across the network.
  • Support and provide informal guidance to junior Budgets Specialists on complex scenarios as needed.
  • Performs related duties
What You Bring to the Team
  • Bachelor's degree or equivalent experience.
  • 4-6 years of site-side clinical research budgeting or trial finance experience, with a focus on complex or high-value negotiations.
  • Deep understanding of site-level clinical trial operations across domestic and international geographies.
  • Proven ability to independently lead complex budget negotiations with sponsors and CROs.
  • Strong judgment in ambiguous situations - able to assess risk, make sound calls, and drive issues to resolution.
  • Excellent communication and stakeholder management skills across internal and external partners.
  • Ability to manage a high-volume, multi-priority workload across regions simultaneously.
  • Self-starter with strong ownership, accountability, and the ability to build or expand on limited structure.
Preferred Qualifications
  • Experience supporting complex multi-country or international clinical research budgets.
  • Familiarity with VAT, currency exchange, and regional payment norms across European markets.
  • Experience using CTMS platforms, particularly RealTime.
  • Familiarity with Medicare Coverage Analysis (MCA) or billing cmpliance.
  • Experience building or improving budgeting processes or tools in a startup or high-growth environment.

How We Work
  • Collaborative and low-ego team environment
  • High ownership and accountability culture
  • Fast-paced and highly iterative growth environment
  • Open communication and continuous learning mindset
  • Mission-driven organization focused on improving patient outcomes
  • Comfortable navigating evolving business priorities and opportunities


Benefits That Support You

We believe great teams do their best work when they feel supported - professionally and personally.
  • Hybrid work environment with in-office collaboration two days per week in either our NYC, Cambridge or Southlake office
  • Comprehensive medical, dental, and vision coverage, with up to 80% of premiums covered by Iterative Health
  • Mental health and wellness support through Spring Health
  • Health HSA or FSA options, and commuter FSA contributions supported by Iterative Health
  • Unlimited PTO, 12 company holidays, and a company-wide shutdown between Christmas and New Years
  • 401(k) program with a company match of up to 3% (up to $3,000 annually)
  • Weekly in-office lunch benefit every Tuesday
  • 100% company-paid short-term and long-term disability coverage
  • Annual wellness and professional development stipend to support your health and growth
  • And more!


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