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The Clinical Research Budgets Analyst plays a critical role in supporting sponsored clinical trials by ensuring the timely and accurate preparation and maintenance of budget templates. This includes conducting comparative reviews of sponsor‑provided budgets and setting up study payment milestones within the Clinical Trial Management System. This position requires strong analytical skills, attention to detail, and the ability to collaborate effectively across multiple research programs and internal teams.
Job Responsibility:
Prepare and maintain accurate budget templates for sponsored clinical trials
Conduct comparative reviews of budgets offered by study sponsors
Set up study payment milestones in the Clinical Trial Management System
Review New Study routing forms and essential study start‑up documents
Perform itemized cost analyses and interpret clinical protocols to develop budget milestones
Provide accurate patient cost descriptions for the Informed Consent Form (ICF) to be submitted to the IRB
Update budgets, milestones, and ICF information as needed to reflect contract or protocol amendments
Work closely with the coverage analysis team, contract analysts, regulatory team, program managers, and internal finance groups
Manage high‑volume workflow across multiple research programs, each with unique processes and requirements
Requirements:
Bachelor's Degree or 4 additional years of related experience
6 years of direct experience in budget development, preferably in clinical trial or medical setting
Nice to have:
Master's Degree in Business or Healthcare Administration
4 years of research grants administration
What we offer:
retirement 401(k) Savings Plan with employer matching
health care benefits (medical, dental, vision)
life insurance
disability insurance
time off benefits (paid parental leave, vacations, holidays, health issues)