Job Description:

• Responsible for the timely and accurate preparation and maintenance of budget templates for sponsored clinical trials
• Review of New Study routing forms and essential study start-up documents
• 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
• Update budget, milestones, and ICF information as necessary per contract/protocol amendments
• Manage large volume workflow across multiple research programs

Requirements:

• 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
• Master's Degree in Business or Healthcare Administration (preferred)
• 4 years of research grants administration (preferred)

Benefits:

• retirement 401(k) Savings Plan with employer matching
• health care benefits (medical, dental, vision)
• life insurance
• disability insurance
• time off benefits (paid parental leave, vacations, holidays, health issues)
• voluntary benefits
• well-being resources