Arrowhead Research

Senior Finance Analyst (Clinical)

Arrowhead Research$100K — $115K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Biological Sciences, Finance, or Accounting, or equivalent clinical research experience (4+ years)
  • 2+ years in clinical trial budgets/contracts or relevant biotechnology/pharmaceutical experience
  • Highly proficient in Microsoft Excel
  • Strong analytical skills with keen attention to detail
  • Excellent communication and organizational skills
  • Ability to effectively engage and tailor communication for various audiences

Responsibilities

  • Review and approve site/vendor budgets and contracts with quality assurance support from Legal
  • Conduct Fair Market Value (FMV) analysis and track budget trends
  • Monitor site payments and ensure compliance with contractual obligations
  • Maintain a master site list for trial documents including CTAs and site budgets
  • Identify Routine Costs in Qualifying Clinical Trials for cost reductions
  • Track site performance to support successful partnerships
  • Reconcile vendor budget payments to ensure accuracy and resolve discrepancies
  • Communicate potential process improvements and serve as a financial liaison to stakeholders

Benefits

  • Competitive salary
  • Excellent benefits package
Full Job Description
The Position Arrowhead seeks a highly energetic & self-motivated Clinical Finance Senior Analyst to engage with CRO's and sites in the review and approval of global site budgets for phase I-IV clinical trials. Incumbent will also assist in the review of site contracts and other study-related documents. The position will report to Arrowhead's Clinical Finance Manager and will work closely with other internal stakeholders to ensure that business objectives and deliverables are met. This is a full-time, onsite position at Arrowhead's Corporate Headquarters in Pasadena, CA. Responsibilities - Review, analyze and approve new and amended site/vendor budgets, including quality assurance of site contracts in tandem with Legal department - Fair Market Value (FMV) analysis and benchmarking of site/vendor budget unit costs, tracking and monitoring trends - Site payment monitoring and tracking alongside CRO's to ensure integrity of contractual obligations - Develop and maintain a master site list to ensure that all trial documents are obtained; including but not limited to clinical trial agreements (CTA), site budgets, informed consents - Assist in identifying Routine Costs in Qualifying Clinical Trials to facilitate site cost reductions - Track and maintain site performance to ensure continuity of successful partnerships - Conduct vendor budget payment reconciliations to validate the accuracy of payments made against approved budgets, identify and resolve discrepancies, and ensure alignment with contractual terms and financial records. - Continuously identify and communicate areas of process improvement - Serve as the business partner to the various internal and external partners, providing sound financial guidance & decision making - Participate in other ad-hoc projects, roles, and workload sharing between Finance as appropriate - Other related duties, as assigned Requirements - Bachelor's degree, preferably in Biological Sciences/Finance/Accounting, or equivalent experience of at least 4 years in the clinical research environment - 2+ years' experience in clinical trial budgets/contracts or related field experience in the biotechnology or pharmaceutical industry - Highly proficient in Microsoft Excel - Ability to gather, analyze and interpret information for completeness and accuracy; excellent attention to detail; excellent organizational skills - Strong communication skills, ability to effectively interact with others at all levels- within and outside of finance. - Ability to tailor communication to the audience to achieve desired results Preferred - CPA/MBA - Expertise in FMV benchmarking and compliance, preferably in GrantPlan - Global/US site-level clinical trial pricing, procedural and administrative experience in reviewing and understanding clinical trial protocols - CPT/HCPCS code competency California pay range $100,000-$115,000 USD Arrowhead provides competitive salaries and an excellent benefit package.

About Arrowhead Research

Arrowhead Research is a biotechnology company that develops RNA interference (RNAi) therapeutics. The company was founded in 2007 and is headquartered in Pasadena, California. Arrowhead's RNAi technology targets specific genes to silence their expression, which can be used to treat a variety of diseases. The company's pipeline includes treatments for liver disease, cancer, and cardiovascular disease. Arrowhead has partnerships with pharmaceutical companies such as Amgen and Janssen Pharmaceuticals. The company has received FDA approval for some of its products and is conducting clinical trials for others.
Learn more about Arrowhead Research
Size
329 employees
Market Cap
$4 billion
Industry
Net Income
-$102.6 million
Founded
2004
5 Year Trend
+50.6%
Revenue
$79.8 million
NASDAQ

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