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Clinical Research Budget Specialist

Remote / Online - Candidates ideally in
Ann Arbor, Washtenaw County, Michigan, 48103, USA
Listing for: Medix™
Full Time, Remote/Work from Home position
Listed on 2026-06-18
Job specializations:
  • Science
    Clinical Research
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below
Position: Clinical Research Budget Specialist 249028

We are looking to add a full time remote Contracts and Budgets Specialist to our growing team. This person will help support a large site network and will assist the Director of Budgets and Contracts- working hand in hand.

Must Have
  • Previous experience in Clinical Trials Budgeting and Contracting
  • Site based Budgeting and Contracting
  • 3 years of related experience, education/training, OR a Bachelor’s degree in related area plus one (1) year of related experience/training.
  • Demonstrated knowledge and experience in negotiating clinical trial budgets with industry sponsors.
  • Extensive knowledge of finance policies, practices and systems, budgeting and reporting techniques, accounting, and bookkeeping.
  • Excellent interpersonal skills including tact, diplomacy, flexibility, and professionalism in dealing with faculty, staff, and industry representatives.
Job Description
  • Assist Director of Budgeting and Contracts with the finalization of live budgets and clinical trial agreements (CTAs) with Sponsors, CROs, vendors, and sites
  • Maintain communication with sponsors through execution of live CTAs. Check for accuracy of information and complete the CTA process through FE – including updating and tracking in appropriate systems
  • Review amendment language and budget to determine changes required based on company requirements with final reviews and approvals through Director.
  • Facilitate budget / contract amendments and communicate effectively with Research Accounting so changes are implemented in the Enterprise CTMS
  • Maintain proper documentation of process and upload appropriate documents in the appropriate systems
  • Assist understanding of budget, contracts, and stipend and budget correspondence for each site
  • Maintain site specific information and documents
  • Comply with current protocols, SOP’s, GCP’s, IRB, and FDA guidelines
  • Performs additional tasks and assist with special projects as needed
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