Role Description

The Clinical Research Financial Analyst is responsible for researching and mapping clinical research financials via reporting from START’s CTMS system and identification and financial reconciliation of expenses from all participating sites and assist START Accounting in billing. This position plays a critical role in ensuring 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. This is a remote role. The annual base salary for this role is $65,000 - $75,000. However, base pay may vary depending on multiple individualized factors including market location, job-related knowledge, skills, and experience. In addition, employees in this role may be eligible for an annual bonus of up to 10% of base earnings.

• 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.
• Other duties may be assigned at any time.

Qualifications

• 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.

Requirements

• Coding knowledge (CPT, HCPCS).
• Three years of CTMS experience, in a healthcare or clinical research setting (Oncology experience) or equal experience of education and knowledge.
• Three years Clinical Trial Management System (OnCore specific) experience.

Benefits

• 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.

Company Description

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.”

As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda – one of the most effective cancer drugs in medical history.

Learn more at STARTresearch.com.