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Glaukos

Medical devices for glaucoma treatment

Reimbursement Liaison - Glaucoma

Full-Time
$143.4k - $179.2k/yr
Mid, Senior
Bachelor's, MBA
Houston, TX, USA+8 moreMore locations: New Orleans, LA, USA | Nashville, TN, USA | Austin, TX, USA | Dallas, TX, USA | Raleigh, NC, USA | Memphis, TN, USA | Charlotte, NC, USA | Columbia, SC, USA
RemoteRemote within the listed territory, with approximately 50% overnight travel and scheduled training or meeting attendance.
Customer Experience & SupportCustomer Education & Training

About the job

Requirements
  • A bachelor's degree in a related field is required; a Master of Business Administration or Master of Public Health is preferred.
  • At least 8 years of experience working with specialty pharmaceuticals or surgical devices is required.
  • At least 3 years of direct reimbursement or healthcare policy experience is required.
  • Experience with reimbursement for physician-administered injectables or medical devices, Category III Current Procedural Terminology codes or miscellaneous J-codes, specialty pharmacy and buy-and-bill acquisition, benefit verifications, prior authorizations, claims assistance, and appeals.
  • Experience with payer and insurance coverage involving Medicare, Medicare Advantage, Veterans Affairs or TRICARE, commercial, and Medicaid plans.
  • Ability to travel adequately to cover the territory, including approximately 50% overnight travel, and attend scheduled training and meetings.
  • A record of achieving objectives and corporate goals with minimal direct supervision.
  • Creativity, situation analysis, problem-solving, and analytical skills.
  • Excellent written, verbal, listening, presentation, and training skills.
  • Leadership and project management skills.
  • Significant experience working with a Patient Service Center or hub.
  • Experience navigating complex authorization processes for specialty medications, orphan diseases, or rare diseases.
  • Ability to educate healthcare professionals about patient support programs, including copay assistance and patient assistance programs.
  • Ability to understand and communicate legal and regulatory parameters related to anti-kickback statutes, fraud and abuse, off-label promotion, and Office of Inspector General guidance for patient assistance programs.
Responsibilities
  • Educate healthcare professionals and office staff on benefit verifications, prior authorization requirements, patient cost-share calculations, and drug acquisition options for patients enrolled in GPS.
  • Collaborate with Patient Support Specialists to identify and eliminate access barriers for patients enrolled in GPS.
  • Respond to healthcare professional questions about coding, payer policy, and approval protocols.
  • Provide expertise on copay assistance for eligible patients enrolled in GPS.
  • Educate practices on the appeals process and on denied or partially paid claims.
  • Lead business reviews and claims reviews for practices.
  • Educate practices on specialty pharmacy and buy-and-bill acquisition options.
  • Monitor reimbursement trends, including policy changes, claim denials, and underpayments, and engage the payer team when patient access may be jeopardized.
  • Maintain expertise in regional and national payer landscapes, clinical requirements, reimbursement policies, utilization-management criteria, prior authorization processes, and appeal requirements.
  • Update customers about policy changes using approved templates and plan approval.
  • Identify coverage gaps, computer errors in policy requirements, and portal-entry challenges that inhibit patient access to care.
  • Manage communications promptly and professionally, ensuring customer needs are met and relevant internal stakeholders are updated.
  • Demonstrate positive leadership without authority to peers, upper management, and other stakeholders by applying account-management expertise.
  • Complete assigned training.
Desired Qualifications
  • Previous sales, district management, field reimbursement, hospital, or medical-practice experience.
  • Eyecare experience.

About the company

Glaukos focuses on ophthalmology by developing and commercializing medical devices and therapies for glaucoma, corneal disorders, and retinal diseases. Its products mainly target surgeons who treat eye conditions, with a core technology in micro invasive glaucoma surgery (MIGS). The company’s MIGS devices, such as the Trabecular Micro Bypass Stent and next-generation iStent, are implanted in the eye to improve outflow of eye fluid and lower intraocular pressure, offering a less invasive option compared with traditional surgeries. Glaukos differentiates itself by pioneering MIGS and bringing the first US-approved MIGS device to market in 2012, continuing to expand its portfolio through research, development, and strategic acquisitions. The company aims to improve patient care by providing safer, effective, and longer-lasting treatment options for glaucoma and related eye diseases, addressing unmet needs in ophthalmology.

Company Size

1,001-5,000

Company Stage

IPO

Headquarters

Aliso Viejo, California

Founded

1998

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Simplify Jobs

Simplify's Take

What believers are saying

  • Q2 2026 revenue hit $185.6 million, up 50%, and guidance rose to $680 million.
  • Epioxa J2789 became effective July 1, 2026, supporting broader payer processing.
  • iDose TR generated about $74 million in Q2 2026 and drives 2026 growth.

What critics are saying

  • Five MACs proposed iDose TR LCDs in Q2 2026; final denials hit 2027.
  • Epioxa billing shifts July 1, 2026, creating Q3 volatility and reimbursement friction.
  • Alcon, Santen, and incumbents can compress adoption if surgeon conversion stalls; thesis weakens fast.

What makes Glaukos unique

  • Glaukos owns MIGS, iDose TR, and Epioxa across glaucoma and keratoconus.
  • iDose TR gained FDA re-administration approval on January 28, 2026.
  • PRESERFLO MicroShunt enrollment finished July 27, 2026, extending beyond MIGS.

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Benefits

Remote Work Options

Growth & Insights and Company News

Headcount

6 month growth

0%

1 year growth

1%

2 year growth

0%
Orange County Business Journal
Oct 9th, 2026
Glaukos reports positive Phase 4 results for iDose TR.

Glaukos reports positive Phase 4 results for iDose TR. Patients receiving iDose TR saw greater reductions in eye pressure Yuika Yoshida October 9, 2026 Aliso Viejo-based Glaukos Corp. today announced positive topline results from a Phase 4 study evaluating its iDose TR glaucoma treatment in patients undergoing cataract surgery. The results met with study's primary endpoint, with iDose TR "demonstrating statistically significant superiority" in reducing intraocular pressure versus cataract surgery alone. The implant is the first long-term sustained release pharmaceutical for the treatment of glaucoma, according to the company. Glaukos also announced yesterday an exclusive licensing agreement with RevOpsis Therapeutics to develop and commercialize an experimental treatment for retinal diseases, including age-related macular degeneration and diabetic eye conditions. The deal also gives Glaukos rights to develop up to four additional retinal therapies. Shares in Glaukos (NYSE: GKOS) were little changed at $161.16 apiece with a $9.5 billion market cap following the announcement. Want more from the best local business newspaper in the country? Sign-up for its FREE Daily eNews update to get the latest Orange County news delivered right to your inbox! One-Year for Only $99 * Weekly in-depth coverage in print and digital formats * Special Features: OC's Wealthiest, Top Priced Home Sales, Giving Guide, OC500, Charity Event Guide, Best Places to Work, Indispensables, Largest Charitable Gifts * The annual Book of Lists: Orange County's top companies across every industry

MarketScreener
Oct 8th, 2026
Glaukos Corporation and RevOpsis Therapeutics, Inc. announce exclusive license agreement to develop and commercialize RO-104, A first-in-class tri-specific biologic for retinal diseases.

Glaukos Corporation and RevOpsis Therapeutics, Inc. announce exclusive license agreement to develop and commercialize RO-104, A first-in-class tri-specific biologic for retinal diseases. Published on 10/08/2026 at 07:00 am EDT S&P Capital IQ Glaukos Corporation announced an exclusive license agreement with RevOpsis Therapeutics, Inc. to develop and commercialize RO-104, a novel tri-specific biologic for the treatment of neovascular age-related macular degeneration (nAMD), diabetic macula edema (DME), diabetic retinopathy (DR), and retinal vein occlusion (RVO). The agreement also grants Glaukos exclusive rights to RevOpsis? proprietary RevMod? platform in geographic atrophy, DME, DR, RVO, and nAMD for the discovery and development of up to four additional next-generation retinal biologic candidates. Financial terms of the agreement were not disclosed. (C) S&P Capital IQ - 2026

Yahoo Finance
Jul 30th, 2026
Glaukos raises 2026 sales guidance to $700M as iDose TR drives 50% Q2 revenue growth

Glaukos reported record second-quarter revenue of $185.6 million, up 50% year over year, driven by strong performance in US glaucoma, international glaucoma and corneal health. The company raised its full-year sales guidance to $680 million–$700 million, up from the prior range of $620 million–$635 million. US glaucoma franchise revenue reached $118.5 million, increasing 64% year over year, with iDose TR contributing approximately $74 million. Glaukos expects iDose TR revenue of roughly $275 million–$280 million in 2026. Corneal health revenue increased 48% to $30.4 million, supported by the Epioxa launch. Gross margin reached approximately 85% as management continues investing in commercialisation and its pipeline whilst targeting cash-flow breakeven.

MarketBeat
Jul 29th, 2026
Glaukos Q2 earnings call highlights.

Glaukos Q2 earnings call highlights. July 29, 2026 Key points. * Record Q2 sales: Glaukos reported $185.6 million in second-quarter revenue, up 50% year over year, driven by strong U.S. glaucoma, international glaucoma and corneal health performance. The company raised its 2026 sales guidance to $680 million-$700 million. * iDose TR led growth: U.S. glaucoma revenue rose 64% to $118.5 million, including approximately $74 million from iDose TR. Glaukos expects iDose TR revenue of roughly $275 million-$280 million in 2026, while Medicare coverage proposals remain under review. * Corneal health and profitability gains: Corneal health revenue increased 48% to $30.4 million, supported by the Epioxa launch, though third-quarter results may be volatile during the transition to its permanent billing code. Gross margin reached about 85%, and management continues investing in commercialization and its pipeline while targeting cash-flow breakeven. * MarketBeat previews top five stocks to own in August. Glaukos NYSE: GKOS reported record second-quarter 2026 consolidated net sales of $185.6 million, up 50% from the prior-year period on a reported basis and 49% on a constant-currency basis, as growth in its U.S. glaucoma, international glaucoma and corneal health businesses exceeded management's expectations. Chairman and CEO Tom Burns said the company raised its full-year net sales guidance to $680 million to $700 million, up from its prior range of $620 million to $635 million. The company cited continued adoption of iDose TR, the launch of Epioxa, and broad-based international growth as drivers of the stronger outlook. iDose TR drives U.S. Glaucoma growth. U.S. glaucoma franchise revenue reached a record $118.5 million in the second quarter, increasing 64% year over year. iDose TR contributed approximately $74 million of that total. Burns said physician interest and adoption of iDose TR continued to grow, supported by its clinical outcomes and what the company views as a shift toward earlier interventional glaucoma care. Glaukos is focused on adding trained surgeons and active accounts, increasing utilization, expanding market access, and growing clinical evidence for the treatment. President and COO Joe Gilliam said Glaukos now expects U.S. glaucoma revenue to grow about 50%, plus or minus, for the full year. The company expects its broader U.S. glaucoma portfolio to post at least low-single-digit growth, while iDose TR revenue is expected to land in a range of roughly $275 million to $280 million in 2026. Gilliam said the second-quarter iDose performance reflected acceleration across Medicare Administrative Contractor regions as well as increased activity among commercial and Medicare Advantage patients. He said the company did not identify material demand pull-forward related to proposed Medicare local coverage determinations, or LCDs. Five of seven Medicare Administrative Contractors issued proposed LCDs for iDose TR during the quarter. Gilliam said Glaukos was encouraged by support from physicians, medical societies and patients during public meetings and comment periods. He said the company believes the evidence supporting iDose TR should lead to a more favorable final policy if LCDs are finalized. Earlier in July, CMS issued proposed 2027 rules that, as drafted, largely maintain 2026 ambulatory payment classifications, facility payments and relative physician fee rates for Glaukos procedures in hospital outpatient and ambulatory surgical center settings, Burns said. International and corneal health performance. International glaucoma revenue was $36.6 million, up 17% reported and 16% on a constant-currency basis. Gilliam said Glaukos now expects low- to mid-teens international glaucoma growth for the full year. Discover more Stock Ratings Screener Management expects foreign-exchange tailwinds to diminish in the second half. The company also cited competitive product trialing and reimbursement headwinds in Germany and Switzerland, though it expects those factors to be partly offset by growth from PRESERFLO and iStent infinite. Corneal health revenue rose 48% to $30.4 million, including about $11 million in Epioxa sales. Epioxa is the company's FDA-approved epithelium-on corneal cross-linking therapy for keratoconus. Gilliam said Glaukos now expects the overall corneal health franchise to grow approximately 20%, plus or minus, in 2026. He cautioned that third-quarter performance could be volatile as the company transitions from Photrexa and a miscellaneous billing code to Epioxa's permanent product-specific J-code, which became effective July 1. "There will be some volatility" during the transition, Gilliam said, though he expects the related issues to begin moving behind the company in the fourth quarter. * O2n systems are deployed at locations serving roughly 85% of the U.S. population, with a pipeline that Glaukos expects could extend reach to approximately 95%. * Access pathways for Epioxa have been established for more than 125 million covered commercial lives, including arrangements involving the five largest U.S. payers. * Glaukos launched a co-pay assistance program for eligible patients and is investing in awareness, referral networks, earlier diagnosis and patient-support programs. Gilliam said the company has been encouraged by the number of patients being submitted for Epioxa approval, though providers and payers are adjusting to the new permanent J-code. He said some institutions and larger groups are more comfortable using a buy-and-bill model, while many community practices are initially relying more heavily on specialty pharmacy distribution. Pipeline and profitability focus. Glaukos said it continues to advance programs across five therapeutic platforms. Its pipeline includes iDose TREX, which is in a Phase II-B/III program; iDose Trio, with a Phase III-B study targeting FDA approval by the end of 2027; and a planned commercial introduction later this year of a keratoconus screening device. The company also said it is preparing a Phase III program for a third-generation customized topographically guided iLink therapy in 2027. In other programs, Glaukos completed enrollment in a 510(k) pivotal study for PRESERFLO MicroShunt and in a Phase II study for demodex blepharitis, with top-line results from the latter expected by year-end. The company is also advancing a first-in-human study of GLK-401 for wet age-related macular degeneration. Chief Financial Officer Alex Thurman said the company was pleased with second-quarter progress across gross margin, operating expenses, the bottom line and cash generation. Gross margin was approximately 85% in the quarter, up about 90 basis points sequentially, driven by a greater revenue contribution from iDose TR and Epioxa. Glaukos maintained its full-year gross-margin target of 84% to 86% and expects modest additional accretion through the remainder of 2026, particularly in the fourth quarter. Thurman said operating expenses are now expected to total around $600 million for the year. While management sees a clearer path toward profitability as revenue grows, Thurman said Glaukos intends to continue investing in commercialization and clinical development to support its product launches and pipeline, while managing the business toward cash-flow breakeven. About Glaukos (NYSE:GKOS). Glaukos Corporation is a medical technology company specializing in the development, manufacturing and commercialization of innovative therapies for patients with glaucoma and other chronic eye diseases. The company's core offerings focus on micro-invasive glaucoma surgery (MIGS), designed to reduce intraocular pressure and manage glaucoma more safely and effectively than traditional surgical approaches. Glaukos's flagship products include the iStent, iStent inject and iStent infinite trabecular micro-bypass stents, which are implanted during cataract surgery to improve aqueous outflow and help control eye pressure. Beyond its MIGS portfolio, Glaukos has expanded into sustained drug-delivery solutions. This instant news alert was generated by narrative science technology and financial data from MarketBeat in order to provide readers with the fastest reporting and unbiased coverage. Please send any questions or comments about this story to [email protected]. Before you consider Glaukos, you'll want to hear this. MarketBeat keeps track of Wall Street's top-rated and best performing research analysts and the stocks they recommend to their clients on a daily basis. MarketBeat has identified the five stocks that top analysts are quietly whispering to their clients to buy now before the broader market catches on... and Glaukos wasn't on the list. While Glaukos currently has a Moderate Buy rating among analysts, top-rated analysts believe these five stocks are better buys. The AI boom extends far beyond the biggest tech names. 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Orange County Business Journal
Jul 27th, 2026
Glaukos completes enrollment for glaucoma implant study.

Glaukos completes enrollment for glaucoma implant study. To support FDA submission Yuika Yoshida July 27, 2026 Glaukos Corp. today announced it has completed enrollment for a 510(k) study of an implantable drainage device designed to lower eye pressure in glaucoma patients. The study enrolled 110 adult patients with primary open-angle glaucoma who failed previous medical and surgical treatment. Results from the study will support a future FDA marketing submission. The device, dubbed Preserflo MicroShunt, is currently approved and commercially available in Canada and Australia. Shares in Glaukos were down 1.3% to $151.63 apiece and an $8.9 billion market cap (NYSE: GKOS). Want more from the best local business newspaper in the country? Sign-up for its FREE Daily eNews update to get the latest Orange County news delivered right to your inbox! One-Year for Only $99 * Weekly in-depth coverage in print and digital formats * Special Features: OC's Wealthiest, Top Priced Home Sales, Giving Guide, OC500, Charity Event Guide, Best Places to Work, Indispensables, Largest Charitable Gifts * The annual Book of Lists: Orange County's top companies across every industry