Department:

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Position Title:

Job Family Group:

Job Description Summary:

Job Description:

Job Duties Outlined:

• Consult with principal investigators project directors regulatory leads and the clinical trial budget manager on budget development for new study submissions as well as budget updates resulting from protocol amendments or other changes in scope.

• Responsible for developing and updating coverage analysis and clinical trial budget; ensure stakeholder review and agreement of draft budgets.

• Review and update financial language in Informed Consents pertaining to patient related costs on clinical studies.

• Consult with other KUMC stakeholders involved with clinical research financial administration including: KUMCRI KU Hospital and the University of Kansas Cancer Center to determine appropriate costing and billing of services.

• Review and revise contract payment terms according to the University of Kansas Cancer Center standard payment term language

• Conduct a final review of budget and payment terms included in contracts to ensure all agreed upon terms are incorporated

• Input budget information into the Clinical Trial Management System (CRIS/Velos).

This job description is not designed to cover or contain a comprehensive listing of activities duties or responsibilities that are required of the employee for this job. It is only a summary of the typical functions of the job not an exhaustive list of all possible job responsibilities tasks duties and assignments. Furthermore job duties responsibilities and activities may change at any time with or without notice.

Work Environment:

• This position may be eligible for a hybrid work schedule after 6 months. Incumbent will work remotely and on campus based on a set departmental schedule based on management approval and must reside in the greater Kansas City metropolitan area.

Required Qualifications:

Work Experience:

• Three years relevant work may be substituted for experience on a year for year basis.

• Previous working knowledge and experience with research/study budgets.

• Familiarity of research billing operations for industry institutional or national group research.

• Experience analyzing and interpreting legal contracts/documents.

Preferred Qualifications:

Licenses/Certifications:

• Professional certification as a clinical research professional or other related certification.

Work Experience:

• Three or more years of clinical researchbudgetdevelopment and negotiation experience. Working knowledge of Medicare Coverage guidelines andFDAregulations relevant to drugs devices and biologics.

• Experience applying knowledge of Medicare Coverage guidelines and FDA regulations relevant to drugs devices and biologics.

Skills:

• Computer skills including Microsoft Work Excel and Access applications

• Attention to detail with analytical and problem-solving skills.

• Multi-tasking and time management skills.

• Interpersonal skills.

• Communication and negotiation skills.

Required Documents:

• Cover Letter AND Resume/CV

Comprehensive Benefits Package: