START Center for Cancer Research

Clinical Research Financial Analyst (Remote)

START Center for Cancer Research · United States · $65K–$80K/yr

Biotechnology Research · 501-1,000 employees

Yesterday
Remote Mid (2-5 yrs) Full-time United States
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About the role

The analyst will research and map clinical research financials using CTMS systems to ensure accurate revenue capture and billing. They will collaborate with sponsors, CROs, and internal accounting teams to reconcile expenses and streamline financial processes.

What they look for

Clinical research financials Financial reconciliation CTMS Billing Revenue cycle management Data mapping MS Office Excel OnCore ARIA Invoicing Financial reporting Contract pricing Clinical trial management

Requirements

Candidates must hold a bachelor's degree in a financial or business-related field. A minimum of one year of experience with Clinical Trial Management Systems (CTMS) is required.

Benefits

401(k) retirement savings plan Annual performance bonus Paid time off Paid holidays Medical coverage Dental coverage Vision coverage Life insurance Disability insurance Employee Assistance Program Flexible FSA HSA plans

Full description

The START Center for Cancer Research (“START”) is the world’s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering "Hope Through Access” to cutting edge trials throughout the United States and Europe.  

 

We are seeking a Clinical Research Financial Analyst who will be responsible for researching and mapping clinical research financials via reporting from START’s CTMS system. This role will assist in identification and financial reconciliation of expenses from all participating sites and assist START Accounting in billing.  This position plays a critical role in ensure that START can fully capture revenue for services provided, in particular for patient visit variations which require specialized coding and tracking to ensure payment by the clinical trial sponsor.

 

The annual base salary for this remote role is $65,000 - $80,000. However, base pay may vary depending on multiple individualized factors including market location, job-related knowledge, skills, and experience.

 

Work Schedule: M-F 8:00AM-5:00PM

Location: Remote

 

Essential Responsibilities:

  • Research and map clinical research financials via Advarra Visit Variation Report to contract pricing.
  • Collaborate with Sponsors and CROs to organize direct invoicing in applicable scenarios.
  • Work with START Accounting to properly identify direct invoicing scenarios and indicate on necessary trackers.
  • Participate in larger reporting projects that assist in identification of rogue or potential erroneous trial expenses.
  • Attend Revenue Cycle task meetings with Leadership and Study Teams in order to align with CTMS visions and changing landscape.
  • Work with Clinical site operations teammates and systems (ARIA) to provide necessary detail for sponsor billing and payment.
  • Assist in streamlining the mapping and reconciliation process to assist with company growth and scaling.

 

 

Required Education and Experience:

  • Bachelor’s degree in financial or business administration field (Accounting, Finance, Business Administration, or similar field).
  • Minimum of one year of CTMS experience, or equal experience of education and knowledge.
  • Clinical Trial Management System (OnCore specific) experience.
  • MS Office Excel and other MS Office programs.

 

 

Preferred Education and Experience:

  • Bachelor’s degree in financial or business administration field (Accounting, Finance, Business Administration, or similar field).
  • Minimum of one year of CTMS experience, or equal experience of education and knowledge.
  • Clinical Trial Management System (OnCore specific) experience.
  • MS Office Excel and other MS Office programs.

 

 

Best-in-Class Benefits and Perks 

We value the time, talent, and dedication our employees bring to START. Our commitment to your well-being and growth is reflected in a competitive compensation package—based on experience—along with comprehensive benefits designed to support you both personally and professionally: 

 

  • 401(k) retirement savings plan with employer match 
  • Eligibility for an annual performance bonus, based on role and company results 
  • Generous paid time off and paid holidays 
  • Comprehensive medical, dental, and vision coverage and optional insurance options 
  • Company paid life and disability insurance for added financial protection 
  • Employee Assistance Program (EAP) providing confidential, no ‑cost support for you and your family from day one 
  • Flexible FSA and HSA plans to support your financial wellness 
  • Commitment to a supportive environment that values balance, wellbeing, and flexibility 
  • We’re committed to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START, you’ll join a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation. 

 

More About START 

START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. START represents the world’s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of “Hope Through Access”.

 

Learn more at STARTresearch.com.  

 

Ready to be part of a team changing the future of cancer treatment? 

Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online. 

 

We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.