CLINICAL RESEARCH BUDGETING ANALYST
3 weeks ago
This role is 100% REMOTE. We CANNOT currently hire remote workers from the following states: CO, HI, MA, NY, OH, PA.
SCHEDULE: 1.0 FTE; 40 hours per week. Day Shift; hours are flexible but generally Monday-Friday, 7:30am-4pm PST.
The Clinical Research Budgets Analyst will be responsible for the timely and accurate preparation and maintenance of budget templates for sponsored clinical trials, including the comparative review against budgets offered by study sponsors and the set-up of study payments milestones in the Clinical Trial Management System. Main responsibilities include, but are not limited to, the review of New Study routing forms and essential study start-up documents, the itemized cost analysis and interpretation of clinical protocols into budgets milestones, provide accurate patient cost descriptions for the ICF to be submitted to the IRB, and update budget, milestones, and ICF information as necessary per contract/protocol amendments.
Additional Responsibilities include but are not limited to:
* Responsible for the development of study budgets from clinical studies protocols and using various software tools. Will complete full evaluation and integration of internal cost during the set-up of a new clinical study; will revise study budgets following revision of study protocols or re-assessment of study cost. Utilize and oversee research rate pricing for PH&S services rendered as part of a clinical trial.
* Communicate with Contracts Analysts to integrate study budget information into clinical trial agreements; may initiate or participate in contract negotiation process.
* Independently initiate or update the coverage determination for each study as applicable and communicate specific study billing structure to the clinical teams and service providers.
* Participate in the administration of study-subject related billing as needed and provide support with the auditing of billing records.
* Collects and maintains complete records and statistics on expenses and payments; regularly monitors compliance of clinical expense to pre-determined budget/billing plan and/or budgets and agreements.
* Establishes and promotes positive working relationships throughout the hospital and between other institutions involved in clinical research.
* Responsible for the set-up of study payments milestones and Billing Instructions grids using Microsoft Applications (Excel) and/or the Clinical Trial Management System.
Required Qualifications:
* 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.
Preferred Qualifications:
* Master's Degree in Business or Healthcare Administration.
* 4 years of Research grants administration.
Why Join Providence?
Providence caregivers are not simply valued - they're invaluable. Join our team at Swedish Research and thrive in our culture of patient-focused, whole-person care built on understanding, commitment, and mutual respect. Your voice matters here, because we know that to inspire and retain the best people, we must empower them.
Our best-in-class benefits are uniquely designed to support you and your family in staying well, growing professionally and achieving financial security. We take care of you, so you can focus on delivering our mission of improving the health and wellbeing of each patient we serve.
Accepting a new position at another facility that is part of the Providence family of organizations may change your current benefits. Changes in benefits, including paid time-off, happen for various reasons. These reasons can include changes of Legal Employer, FTE, Union, location, time-off plan policies, availability of health and welfare benefit plan offerings, and other various reasons.
Apply Today Applicants that meet qualifications will receive a text with some additional questions from our Modern Hire system.
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