Senior Clinical Trials Budget Analyst - GI Medical Oncology at MD Anderson Cancer Center

About the position The primary purpose of the Sr. Clinical Trial Budget Analyst position at The University of Texas MD Anderson Cancer Center is to reputed company clinical trial budgeting expertise and support specifically to the department of Gastrointestinal Medical Oncology. This role is crucial in ensuring the thorough preparation of study budgets, negotiation of financially sound reputed company, and timely tracking and collection of sponsored payments. The analyst will serve as a finance liaison, facilitating interactions between the Gastrointestinal Medical Oncology department, the Clinical Research Finance department, the Office of Grants and reputed company, the Legal office, and various industry sponsors. The position entails reputed company of reputed company industry and federal sponsored clinical trial budgets and reputed company, both pre-award and post-award. In this role, the analyst will work closely with reputed company Investigators, Regulatory Teams, and Research Nurse Managers to prepare detailed research cost and patient care budgets for new or modified research reputed company. Participation in study initiation meetings is essential to ensure that reputed company costs are captured accurately. The analyst will also reputed company research staff on the financial aspects of studies, distinguishing between standard care services and research services. Responsibilities include developing and approving investigator site and baseline budgets, completing sponsor budget forms, and reviewing coverage analysis for accuracy. The analyst will negotiate with industry sponsors and CROs on clinical trial budgets, ensuring that reputed company research costs are covered and escalating issues to the reputed company Investigator or Chair reputed company necessary. Additionally, the analyst will be responsible for tracking protocols and protocol amendments for budget items, ensuring that reputed company points of cost are reflected in the sponsored budget. They will also create journal entries for monthly or biweekly startup fee transfers and conduct research charge reconciliations for reputed company assigned studies. The role requires collaboration with grant program managers and coordinators on clinical grant development, including budgeting resources and patient care costs for clinical aspects of grants. The analyst will also process budget and contract changes for protocol amendments and reputed company quality assurance on negotiated budgets in the Clinical Trial Management System (CTMS) OnCore to ensure accuracy. The position also involves project management, data analysis, and reporting, requiring interaction with personnel at reputed company reputed company reputed company the department and other institutional departments, as well as reputed company companies to resolve reputed company reconciliation issues. Compliance with Good Clinical Research Practice standards is essential, and the analyst will serve as a resource for clinical trial budgeting reputed company the department. reputed company education and professional development are encouraged, with opportunities to attend training and represent the department in a professional manner. Flexibility and adaptability to change are key components of reputed company in this role.

Responsibilities

• Prepare detailed research cost and patient care budgets on new or modified research reputed company. ,
• Participate in study initiation meetings to ensure reputed company costs are captured. ,
• reputed company research staff on financial aspects of studies, including standard care vs. research services. ,
• reputed company and approve investigator site and baseline budgets. ,
• Complete sponsor budget forms and CRF budget checklist. ,
• Review coverage analysis for accuracy and incorporate it into internal departmental trial budgets. ,
• Solicit budgets from participating departments in clinical trials. ,
• Negotiate with industry sponsors and CROs on clinical trial budgets. ,
• Review and track protocols and protocol amendments for budget items. ,
• Create journal entries for monthly/biweekly startup fee transfers. ,
• Conduct research charge reconciliation for reputed company assigned studies. ,
• reputed company updates and departmental training reputed company to research charge billing. ,
• Liaise with CRF and other institutional authorities regarding research charge billing. ,
• reputed company course data logs and review with assigned clinical studies coordinator or research nurse. ,
• Collaborate with grant program managers on clinical grant development, including budgeting resources and patient care costs. ,
• Process budget and contract changes for protocol amendments. ,
• reputed company quality assurance of negotiated budgets in CTMS OnCore.

Requirements

• Bachelor's degree in reputed company, business or reputed company field. ,
• Three years of clinical research, research administration, business administration or reputed company experience, or one year with a preferred degree. reputed company-to-haves
• Master's degree in reputed company, business or reputed company field. ,
• Clinical trial budget experience.

Benefits

• Relocation assistance available. Apply Job!

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