Budget Analyst I (Clinical Trials)
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Position Details
Position Information Recruitment/Posting Title Budget Analyst I (Clinical Trials) Job Category Staff & Executive Department Cancer Institute of New Jersey Overview Through our science, our evidence-based actions, our openness, and our respect for those we serve, we will advance cancer-focused research worldwide and reduce the burden of cancer in our catchment area. By engaging with and empowering our exceptionally diverse populations, and addressing their questions and fears, we will engender hope for cancer patients and their families and play a critical role in strengthening the fabric of our communities by gaining and protecting their trust and providing access to the outstanding oncology care each person deserves. Our mission is to accelerate scientific discovery focused on understanding cancer, innovating cancer treatment, and improving cancer prevention; to provide outstanding, novel, and compassionate patient care; to provide evidence-based and culturally informed education to physicians, nurses, researchers, staff, and the community; and to achieve cancer health equity in our state through outreach to and engagement of our extraordinarily diverse communities. Curiosity and Discovery, Integrity, Collaboration, Cultivating Diversity, Respect and Caring, Perseverance. Posting Summary Rutgers, The State University of New Jersey is seeking a Budget Analyst I (Clinical Trials) within the Rutgers Cancer Institute of New Jersey. The Budget Analyst I (Clinical Trials) is responsible for preparing, maintaining, and negotiating budgets related to clinical trial activities. A key function of this position is to perform prospective reimbursement analysis according to CMS National Coverage Determination Decisions and all applicable billing regulations, third party requirements, industry standards, intern al policies and procedures, and University policy. This position will work in conjunction with other departments at Rutgers Cancer Institute of New Jersey, as well as representatives from other institutions of higher education, sponsors, attorneys, governmental agencies, philanthropic organizations and principal investigators as a necessary function of the job. Among the key duties for this position are the following:- Requests clinical trial budgets and contracts documents from sponsors and CROs.
- Reviews clinical trial protocols and develops internal budgets. Prepares clinical trial budget documents and memos as requested.
- Interfaces with various departments in the institution and sponsors when appropriate to negotiate budgets.
- Facilitates clinical trial billing administrative start-up.
- Clinical Research Billing and Regulatory Compliance.
- Bachelor's Degree in Accounting, Finance, Business Administration or a related field; plus a minimum of three (3) years of experience in the maintenance and review of budgetary and fiscal records including experience with computer based accounting systems in a healthcare environment.
- Equivalent experience, education and/or training may be substituted for the degree requirements.
- Maintains working knowledge of CMS, DHHS, FDA, OHRP, NIH, OIG, HIPPA and IRB required.
- Demonstrates excellent interpersonal, oral and written communication skills.
- Strong organizational and administrative skills; detail oriented and solid computer skills.
- Must be computer literate with proficiency and working knowledge of database and reporting tools such as Microsoft Word, Excel, Access, PowerPoint and ONCORE.
- Experience with clinical contracts, budget development, variance analysis and research of financial data and transactions preferred.
- Experience in clinical research conduct, administration or coordination preferred.
- Knowledge of regulatory, financial and administrative requirements of third party billing for clinical trials and accounting principles for research preferred.
- Experience or training in clinical research budgeting, financial management and/or coding preferred.
- Maintains thorough working knowledge of regulatory requirements, Good Clinical Practices (GCP) experience strongly desired.
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