Swedish
Clinical Research Budgeting Analyst - Clinical Trials
Swedish, Olympia, Washington, United States
Clinical Research Budgeting Analyst - Clinical Trials
Remote position. 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 setup of study payments milestones in the Clinical Trial Management System. Overview
Join to apply for the Clinical Research Budgeting Analyst - Clinical Trials role at Swedish. Responsibilities
Prepare and maintain budget templates for sponsored clinical trials. Conduct comparative reviews against sponsor budgets. Set up study payment milestones in the Clinical Trial Management System. Review New Study routing forms and essential study start-up documents. Perform itemized cost analysis and interpret clinical protocols into budget milestones. Provide accurate patient cost descriptions for the informed consent form (ICF) to be submitted to the IRB. Update budget, milestones, and ICF information as necessary per contract or protocol amendments. Qualifications
Required: Bachelor\'s Degree or 4 additional years of related experience. Required: 6 years of direct experience in budget development, preferably in a clinical trial or medical setting. Preferred: Master\'s Degree in Business or Healthcare Administration. Preferred: 4 years of research grants administration. Note: This description reflects the responsibilities and qualifications for the role and does not include all external details from the original posting.
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Remote position. 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 setup of study payments milestones in the Clinical Trial Management System. Overview
Join to apply for the Clinical Research Budgeting Analyst - Clinical Trials role at Swedish. Responsibilities
Prepare and maintain budget templates for sponsored clinical trials. Conduct comparative reviews against sponsor budgets. Set up study payment milestones in the Clinical Trial Management System. Review New Study routing forms and essential study start-up documents. Perform itemized cost analysis and interpret clinical protocols into budget milestones. Provide accurate patient cost descriptions for the informed consent form (ICF) to be submitted to the IRB. Update budget, milestones, and ICF information as necessary per contract or protocol amendments. Qualifications
Required: Bachelor\'s Degree or 4 additional years of related experience. Required: 6 years of direct experience in budget development, preferably in a clinical trial or medical setting. Preferred: Master\'s Degree in Business or Healthcare Administration. Preferred: 4 years of research grants administration. Note: This description reflects the responsibilities and qualifications for the role and does not include all external details from the original posting.
#J-18808-Ljbffr