Full-Time

Manager – Payer Analytics & Operations

Posted on 5/9/2026

Travere Therapeutics

Travere Therapeutics

501-1,000 employees

Develops and commercializes rare-disease therapies

Compensation Overview

$116k - $151k/yr

+ Short-Term Incentive + Stock-Based Compensation

San Diego, CA, USA

In Person

Face-to-face work in San Diego; 10-20% travel domestically and internationally.

Category
Business & Strategy (2)
,
Required Skills
Data Analysis
Requirements
  • Bachelor’s degree required.
  • Masters / MBA preferred. Equivalent combination of education and applicable job experience may be considered.
  • 5+ years of relevant work experience in an analyst capacity in the pharmaceutical industry.
  • All positions have an essential job function to be able to perform face to face work with colleagues and/or onsite in San Diego.
  • Ability to travel 10% to 20% domestic and internationally.
Responsibilities
  • Analyze payer coverage, reimbursement, and policy dynamics across Commercial, Medicare, and Medicaid channels.
  • Assess access barriers (e.g., prior authorizations, step edits, denials) and quantify impact to patient access.
  • Generate insights from claims, hub, and patient services data to identify trends in utilization and adherence.
  • Monitor and report on key performance indicators such as time-to-fill, approval rates, and therapy persistence.
  • Develop and deliver recurring insights to inform Patient Access strategy and leadership decision-making.
  • Translate complex datasets into clear, actionable recommendations for cross-functional stakeholders.
  • Identify risks and opportunities related to payer performance and patient access.
  • Own and evolve dashboards supporting payer performance, field reimbursement, and patient access.
  • Partner with IT and data engineering teams to enhance reporting capabilities, automation, and ensure data accuracy, consistency, and usability across systems.
  • Serve as the primary point of contact for external data vendors (e.g., claims aggregators, data providers)
  • Support payer contracting strategy through data-driven insights and scenario analyses.
  • Evaluate impact of payer agreements on access, utilization, and financial performance.
  • Partner with Pricing & Contracting to inform decision-making for both in-line and pipeline products.
  • Contribute to business planning cycles, including quarterly reviews and long-range planning and act as a strategic thought partner to cross-functional stakeholders
  • Lead multiple analytical projects by implementing solutions, ensuring progress per timelines and scope, and coordinating readout of results.
  • Demonstrate strong biopharma understanding and business intelligence to present data to get a clear understanding of our current performance and trends across multiple perspectives.
  • Demonstrate attention to detail, validating and verifying data for accuracy and completeness prior to publishing materials to business stakeholders. Communicate and work with team members to mitigate data variances or challenges should they occur.
  • Ensure all reporting and analytics activities are conducted in accordance with ethical compliance guidelines.
Desired Qualifications
  • Masters / MBA preferred.
  • Expert level user and modeler within Microsoft Excel.
  • Alteryx and/or SAS/Power BI experience is a plus.
  • Strong PowerPoint and presentation skills preferred.
  • Expertise in analytics, particularly in technical data curation, integration across multiple data sets, data structuring, and data manipulation skills.
  • Strong analytical reasoning and problem-solving capabilities with demonstrated abilities to think creatively and strategically to solve and answer key business questions/problems.
  • Excellent interpersonal and collaborative skills, with a professional demeanor, with the ability to interact with all levels of management, colleagues within other departments and vendors.
  • Excellent communication and presentation skills with the ability to present at a management level and the capability to dive into details when needed.
  • Travel requirement of 10% to 20% domestically and internationally is noted as part of job.

Travere Therapeutics develops and commercializes therapies for rare diseases, especially kidney and metabolic disorders. It has commercial products Thiola and Thiola EC for cystinuria and Chenodal for gallstones, with a pipeline that includes sparsentan for focal segmental glomerulosclerosis and IgA nephropathy. The company generates revenue from the sale of its products and supports patients through a dedicated patient assistance program. Its approach centers on identifying and delivering treatments for rare diseases, combining commercialization with ongoing drug development.

Company Size

501-1,000

Company Stage

IPO

Headquarters

San Diego, California

Founded

2008

Simplify Jobs

Simplify's Take

What believers are saying

  • FILSPARI Q1 2026 sales hit $105.2 million, up 88% year-over-year.
  • FSGS approval expands US addressable market beyond 100,000 patients.
  • Chugai submits sparsentan NDA in Japan 2026, triggering milestone payments.

What critics are saying

  • Robbins Geller investigates Travere for securities violations since January 2026.
  • Ligand claims 9% royalty on all worldwide FILSPARI sales.
  • Novartis atrasentan Phase III threatens 20-30% FILSPARI market share.

What makes Travere Therapeutics unique

  • FILSPARI is first FDA-approved therapy for FSGS in patients aged 8 and older.
  • FILSPARI leads IgAN market as most prescribed FDA-approved medicine.
  • Pegtibatinase advances as novel Phase 3 enzyme replacement for classical homocystinuria.

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Benefits

Health Insurance

Life Insurance

Disability Insurance

401(k) Company Match

Paid Vacation

Wellness Program

Company Equity

Company News

Yahoo Finance
Apr 14th, 2026
Travere's FILSPARI receives FDA approval for FSGS, earns Ligand 9% royalty on sales

Ligand Pharmaceuticals' partner Travere Therapeutics has received FDA approval for FILSPARI (sparsentan) to treat focal segmental glomerulosclerosis (FSGS) in adult and paediatric patients aged eight and older without nephrotic syndrome. FILSPARI becomes the first and only FDA-approved medicine for FSGS, a rare kidney disorder and leading cause of kidney failure. The approval expands FILSPARI beyond IgA nephropathy, where it is already the most commonly prescribed FDA-approved medicine. Ligand is entitled to a 9% royalty on worldwide net sales. Travere estimates the addressable US population exceeds 30,000 individuals with FSGS without nephrotic syndrome. In the Phase 3 DUPLEX Study, FILSPARI demonstrated a statistically significant 48% reduction in proteinuria compared to 27% for irbesartan in patients without nephrotic syndrome.

Yahoo Finance
Apr 13th, 2026
FDA fully approves FILSPARI for FSGS, first treatment for rare kidney disease affecting 30K US patients

Travere Therapeutics announced that the FDA has granted full approval for FILSPARI (sparsentan) to reduce proteinuria in adults and children aged 8 years and older with focal segmental glomerulosclerosis (FSGS) who do not have nephrotic syndrome. FILSPARI is the first and only FDA-approved medicine for FSGS. The approval expands FILSPARI's addressable population to more than 100,000 patients in the US, including over 30,000 with FSGS. The drug is already the most commonly prescribed FDA-approved medicine for IgA nephropathy. In the Phase 3 DUPLEX Study, FILSPARI demonstrated a statistically significant 46% reduction in proteinuria compared to 30% for irbesartan. In patients without nephrotic syndrome specifically, the reduction was 48% versus 27%. The medicine was generally well tolerated across adult and paediatric patients.

The Motley Fool
Jan 25th, 2026
Palisades Investment Initiated a Position in Travere Therapeutics Worth Over $5 Million. Is the Stock a Buy? | The Motley Fool

This biopharma firm targets rare diseases with both approved therapies and a pipeline of clinical-stage treatments.

The Motley Fool
Jan 24th, 2026
Palisades Investment buys $5.3M stake in Travere Therapeutics as shares surge 51%

Palisades Investment Partners initiated a new position in Travere Therapeutics worth $5.26 million, acquiring 137,768 shares in the fourth quarter of 2025, according to an SEC filing. The stake represents 1.99% of the fund's $264.72 million in reportable US equity assets. Travere Therapeutics, a biotechnology company specialising in rare disease therapies, has seen its shares rise 50.89% over the past year to $27.87. The company's revenue surged to $164.9 million in the third quarter, driven by a 155% year-over-year increase in sales of its FILSPARI drug to $90.9 million. The timing of Palisades' investment coincided with FDA review of FILSPARI for potential expanded approval in focal segmental glomerulosclerosis treatments, suggesting confidence in the company's growth prospects.

GlobeNewswire
Jan 13th, 2026
TVTX ALERT: Investigation Launched into Travere Therapeutics, Inc., RGRD Law Attorneys Encourage Investors and Potential Witnesses to Contact Law Firm

TVTX ALERT: investigation launched into Travere Therapeutics, Inc., RGRD law attorneys encourage investors and potential witnesses to contact law Firm. SAN DIEGO, Jan. 13, 2026 (GLOBE NEWSWIRE) - Robbins Geller Rudman & Dowd LLP is investigating potential violations of U.S. federal securities laws involving Travere Therapeutics, Inc. (NASDAQ: TVTX). If you have information that could assist in the Travere investigation or if you are a Travere investor who suffered a loss and would like to learn more, you can provide your information here: You can also contact attorney J.C. Sanchez of Robbins Geller by calling 800/449-4900 or via e-mail at [email protected]. THE COMPANY: Travere is a biopharmaceutical company that develops therapies for people living with rare kidney and metabolic diseases in the United States. THE INVESTIGATION: Robbins Geller is investigating whether Travere and certain of its top executives made materially false and/or misleading statements and/or omitted material information regarding Travere's business and operations. ABOUT ROBBINS GELLER: Robbins Geller Rudman & Dowd LLP is one of the world's leading law firms representing investors in securities fraud and shareholder litigation. Our Firm has been ranked #1 in the ISS Securities Class Action Services rankings for four out of the last five years for securing the most monetary relief for investors. In 2024, we recovered over $2.5 billion for investors in securities-related class action cases - more than the next five law firms combined, according to ISS. With 200 lawyers in 10 offices, Robbins Geller is one of the largest plaintiffs' firms in the world, and the Firm's attorneys have obtained many of the largest securities class action recoveries in history, including the largest ever - $7.2 billion - in In re Enron Corp. Sec. Litig. Please visit the following page for more information: Past results do not guarantee future outcomes. Services may be performed by attorneys in any of our offices.