
Clinical Research Budgeting Analyst – Clinical Trials
Posted Sep 11

Posted Sep 11
This is a fully remote position, open to applicants in Alaska, +5 more states.
• Prepare and oversee budgets for sponsored clinical trials.
• Conduct comparative reviews of budgets proposed by study sponsors.
• Establish payment milestones and Billing Instructions grids using Velos and/or Microsoft Excel.
• Evaluate New Study routing forms and critical study start-up documents.
• Analyze detailed costs and convert clinical protocols into budget milestones.
• Provide descriptions of patient costs for informed consent forms submitted to the IRB.
• Revise budgets, milestones, and ICF information in response to contract or protocol amendments.
• Create and modify study budgets while incorporating internal costs during the setup of new studies.
• Utilize and manage research rate pricing for clinical trial services at Providence Health & Services.
• Collaborate with Contracts Analysts to incorporate budget details into clinical trial agreements.
• Initiate or take part in contract negotiations.
• Start or update coverage determinations and communicate the study billing structures.
• Aid in study-subject billing administration and audit billing records.
• Maintain comprehensive records and statistics on expenses and payments.
• Ensure compliance of clinical expenses with budgets, billing plans, and agreements.
• Work closely with research departments, hospital teams, other institutions, contract analysts, regulatory teams, program managers, and internal finance groups.
• Support physician investigators and create internal cost analyses for investigator-initiated trials.
• Bachelor's Degree or 4 additional years of relevant experience.
• 6 years of direct experience in budget development, ideally in a clinical trial or medical environment.
• Preferred: Master's Degree in Business or Healthcare Administration.
• Preferred: 4 years of experience in research grants administration.
• Proficiency in Microsoft Applications, particularly Excel.
• Familiarity with the Clinical Trial Management System (Velos).
• Ability to interpret clinical study protocols and formulate budgets.
• Capability to manage high-volume workflows across multiple research programs.
• Retirement 401(k) Savings Plan with employer matching.
• Medical, dental, and vision health care benefits.
• Life insurance.
• Disability insurance.
• Paid parental leave.
• Vacation and holiday time off.
• Time off for health-related issues.
• Voluntary benefits.
• Well-being resources.
• An inclusive workplace with equal opportunities for advancement.
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