Full-Time

Endocrine Account Manager

Updated on 9/4/2026

BridgeBio

BridgeBio

1,001-5,000 employees

Develops therapies for genetic diseases

Compensation Overview

$155k - $210k/yr

+ Annual performance bonus + Company equity

Indianapolis, IN, USA

Hybrid

Significant travel is required across Indiana, Lexington, and Louisville.

Bachelor's, MBA

Category
Sales & Account Management (1)
Required Skills
Data Analysis

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Requirements
  • 8-10 years of successful experience in the pharmaceutical industry, including 4+ years in endocrine disease and/or nephrology.
  • A Bachelor of Science or Bachelor of Arts degree is required.
  • A track record of successfully launching new products and/or new indications into highly competitive and/or new markets.
  • Strong leadership, planning and organization, analytics, business acumen, decision-making, and problem-solving skills.
  • Ability to prioritize and execute on the plan.
  • Proven leadership skills with a history of holding oneself to a high level of accountability.
  • Ability to influence without authority, internally and externally.
  • Excellent written and oral communication skills.
  • Excellent skills using remote technology and artificial intelligence to engage with customers and analyze business opportunities.
  • Adherence to the company's high ethical standards.
  • Willingness to travel significantly across a large geography.
Responsibilities
  • Meet and/or exceed sales goals in an assigned territory by developing, implementing, and executing an integrated territory business plan encompassing key customer targets.
  • Demonstrate subject matter expertise concerning scientific and clinical information for Encaleret.
  • Take a customer-centric approach and engage customers in clinically relevant discussions using approved materials.
  • Analyze sales and targeting data to identify opportunities for business growth or areas of concern in the territory.
  • Own territory business planning and execute key company initiatives.
  • Adhere to company guidelines and demonstrate honesty, integrity, trust, respect, and accountability while performing responsibilities in accordance with company policies, procedures, and applicable state and federal rules and regulations.
  • Partner compliantly with Medical Science Liaisons, Field Reimbursement, Patient Access, HUB, and other key cross-functional team members to develop strategies that ensure high customer satisfaction.
  • Develop and implement a dynamic territory business plan by analyzing the ADH1 market in the territory to drive business.
  • Develop, nurture, and maintain professional relationships with targeted healthcare providers, including physicians, medical staff, key personnel, and multidisciplinary staff.
  • Anticipate potential business challenges, adjust priorities as needed, demonstrate flexibility, and develop solutions to address challenges.
  • Maintain exceptional proficiency in selling skills, clinical, market, and product knowledge, and the business environment of the territory.
  • Collaborate with peers and company personnel to ensure corporate objectives and initiatives are achieved.
  • Plan and organize the schedule effectively to maximize efficiency and use of time to accomplish goals and objectives.
  • Act as an ambassador on behalf of BridgeBio and present a professional image while representing the company, products, and people with integrity and respect.
  • Ensure that all activities follow applicable regulations, compliance requirements, and pharmaceutical guidelines.
Desired Qualifications
  • Rare disease experience.
  • A Master of Business Administration degree.

BridgeBio Pharma develops medicines for genetic diseases through a decentralized subsidiary model, with each subsidiary focused on a specific disease while sharing central resources. It advances multiple drug programs at once by using genome sequencing, molecular biology, and patient data to identify targets and translate research into therapies. Therapies target the underlying genetic causes to create disease-modifying treatments, and BridgeBio monetizes via licensing, partnerships, and eventual commercialization of approved drugs. The company differentiates itself by its independent subsidiaries with centralized support, data-driven decision making, and a culture of radical transparency, all to accelerate discovery and bring therapies to patients faster.

Company Size

1,001-5,000

Company Stage

IPO

Headquarters

Palo Alto, California

Founded

2014

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Simplify Jobs

Simplify's Take

What believers are saying

  • Q2 2026 revenue reached $243.7 million; Attruby sales hit $222.4 million.
  • Attruby first-half 2026 sales reached $403 million, with treatment-naive share still rising.
  • ENCAleret and infigratinib are under FDA review, creating multiple launch catalysts through 2027.

What critics are saying

  • Attruby concentration is extreme; any reimbursement or safety slip before 2027 crushes growth.
  • BBP-418 faces a November 27, 2026 FDA decision; a CRL would damage credibility.
  • Tafamidis remains the entrenched ATTR-CM rival; payers can force step-edits and slow switching.

What makes BridgeBio unique

  • Acoramidis/Attruby is approved globally and showed 54-month survival benefit at ESC 2026.
  • BridgeBio’s decentralized model pushes three NDAs simultaneously: BBP-418, encaleret, infigratinib.
  • BBP-418 could become the first approved therapy for LGMD2I/R9, per May 2026 FDA filing.

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Benefits

Health Insurance

Performance Bonus

Company Equity

Unlimited Paid Time Off

Growth & Insights and Company News

Headcount

6 month growth

-1%

1 year growth

-3%

2 year growth

1%
Ticker Report
Sep 2nd, 2026
Lionsbridge Wealth Management LLC Makes New Investment in BridgeBio Pharma, Inc. $BBIO

Lionsbridge Wealth Management LLC acquired a new position in BridgeBio Pharma, Inc. (NASDAQ:BBIO – Free Report) in the 2nd quarter, according to the company in its most recent Form 13F filing with the Securities and Exchange Commission (SEC). The institutional investor acquired 9,453 shares of the company’s stock, valued at approximately $704,000. A number of […]

Africa Daily Journal
Sep 2nd, 2026
BridgeBio to present new data on the impact of Oral Infigratinib on medical complications in achondroplasia at the Annual ESPE Meeting 2026.

BridgeBio to present new data on the impact of Oral Infigratinib on medical complications in achondroplasia at the Annual ESPE Meeting 2026. PALO ALTO, Calif., Sept. 02, 2026 (GLOBE NEWSWIRE) - BridgeBio Pharma, Inc. (Nasdaq: BBIO) ("BridgeBio" or the "Company"), a commercial-stage, multi-product biopharmaceutical company focused on developing medicines for genetic conditions, announced today that one late-breaking oral presentation on the impact of oral infigratinib on medical complications in achondroplasia from PROPEL 3 will be shared at the Annual European Society for Paediatric Endocrinology (ESPE) Meeting 2026, taking place in Marseille, France on September 8-10, 2026. In addition to the late-breaking oral presentation, two posters and one eposter will be shared on longer-term data for oral infigratinib in achondroplasia, PROPEL I&T-an ongoing Phase 2/2b study in children under 3 years old with achondroplasia, and qualitative research on the impacts of hypochondroplasia. BridgeBio is committed to exploring the potential of oral infigratinib on wider medical and functional impacts of achondroplasia, hypochondroplasia and other skeletal dysplasia conditions, which hold significant unmet needs for families. Late-Breaking Oral Presentation: A Randomized Controlled Trial of Oral Infigratinib in Children with Achondroplasia: Results from the PROPEL 3 Study Presenter: Julie Hoover-Fong, M.D., Ph.D., Johns Hopkins University, U.S. Date: Wednesday, September 9 at 10:00 am CEST Posters: Longer-Term Efficacy and Safety Results of Infigratinib in Children with Achondroplasia Presenter: Melita Irving, M.D., Guy's and St Thomas' NHS Foundation Trust, London, UK PROPEL Infant and Toddler: Study Design and Ongoing Enrollment of a Phase 2/2b Study of Infigratinib in Children under 3 Years Old with Achondroplasia Presenter: Melita Irving, M.D., Guy's and St Thomas' NHS Foundation Trust, London, UK ePoster: Potential Medical Challenges and Functional Impacts of Hypochondroplasia: Qualitative Interviews with Children and Parents Presenter: Melita Irving, M.D., Guy's and St Thomas' NHS Foundation Trust, London, UK About Achondroplasia Achondroplasia is the most common cause of disproportionate short stature, affecting approximately 55,000 people in the U.S. and European Union (EU), including up to 10,000 children and adolescents with open growth plates. Achondroplasia impacts overall health and quality of life, leading to medical complications such as obstructive sleep apnea, middle ear dysfunction, kyphosis, and spinal stenosis. The condition is uniformly caused by an activating variant in FGFR3. About Oral Infigratinib Oral infigratinib is an investigational small molecule designed to inhibit FGFR3 signaling and target skeletal dysplasias, including achondroplasia and hypochondroplasia, at their source. Overactivating FGFR3 pathogenic variants drive downstream MAPK and STAT1 signaling that aberrates growth plate development, thereby causing disproportionate short stature and the potential for serious health complications. Oral infigratinib improves bone growth by decreasing the overactivity of FGFR3. About BridgeBio BridgeBio exists to develop transformative medicines for genetic conditions. Millions of people worldwide living with genetic conditions lack treatment options, often because drug development for small patient populations can be commercially challenging. Africa Daily Journal aim to bridge the gap between advancements in genetic science and meaningful medicines for underserved patient populations. Its decentralized, hub-and-spoke model is designed for speed, precision, and scalability. Autonomous and empowered teams focus on individual conditions, while a central hub provides the clinical, regulatory, and commercial capabilities needed to bring innovation to market. For more information, visit bridgebio.com and follow Africa Daily Journal on LinkedIn, X, Facebook, Instagram, YouTube, and TikTok. BridgeBio Media Contact: Kaitlyn Reilly, Director, Communications [email protected] (650) 789-8220 BridgeBio Investor Contact: Kristen Kelleher, Director, Investor Relations [email protected] Legal Disclaimer: EIN Presswire provides this news content "as is" without warranty of any kind. Africa Daily Journal do not accept any responsibility or liability for the accuracy, content, images, videos, licenses, completeness, legality, or reliability of the information contained in this article. If you have any complaints or copyright issues related to this article, kindly contact the author above.

Yahoo Finance
Aug 30th, 2026
Acoramidis shows potential cardiac disease reversal in ATTR-CM patients, adding 65 days alive out of hospital

BridgeBio Pharma presented new analyses from its Phase 3 ATTRibute-CM study of Attruby (acoramidis) for transthyretin amyloid cardiomyopathy at the European Society of Cardiology Congress 2026. The findings were simultaneously published in the European Journal of Heart Failure. Acoramidis is the first therapy shown to potentially reverse cardiac structural disease progression and functional decline through 42 months based on CMR imaging. Up to half of patients showed clinically meaningful improvement in cardiac function in the completer analysis. Patients treated with acoramidis had 65 additional days alive and out of hospital by Month 36 versus baseline placebo patients. The drug demonstrated long-term efficacy and safety through 54 months across variant ATTR-CM subgroups. Acoramidis is an orally administered, near-complete transthyretin stabiliser.

Yahoo Finance
Aug 25th, 2026
BridgeBio surges 24% in three months as Attruby sales hit $403M amid upcoming FDA decisions

BridgeBio Pharma shares have risen 24% in the past three months, significantly outperforming the S&P 500's 0.7% gain over the same period. The rally extends a 71.4% advance over the past year. Attruby generated $403 million in US sales during the first half of 2026, following $362.4 million in 2025. The drug continued gaining share among treatment-naive patients whilst diagnosed ATTR-CM patients in the United States exceeded 50,000 in 2025. The company faces an FDA decision for BBP-418 by 27 November 2026, with additional regulatory decisions expected for encaleret on 8 May 2027 and infigratinib in early to mid-2027. BBIO trades at 12 times forward enterprise value-to-sales, compared with 2.9 times for its industry peers.

Cardio Health Alliance
Aug 24th, 2026
BridgeBio joins CardioHealth Alliance as a new life science partner to advance evidence-based prevention and care.

BridgeBio joins CardioHealth Alliance as a new life science partner to advance evidence-based prevention and care. Posted on August 24, 2026 by A M The CardioHealth Alliance welcomes BridgeBio as a new life science partner, further strengthening the Alliance's work to advance evidence-based solutions for the prevention and care of cardiovascular, renal, and metabolic diseases. BridgeBio is a biopharmaceutical company focused on developing transformative medicines for patients with genetic diseases, like transthyretin amyloid cardiomyopathy (ATTR-CM). Through its support of the CardioHealth Alliance, BridgeBio will help advance collaborative efforts to address gaps in cardiovascular care and accelerate the translation of research insights into real-world practice. "BridgeBio was founded to close the gap between genetic discovery and patient care, and cardiovascular disease is where this gap can cost the most lives. Closing this gap requires the kind of cross-disciplinary innovation and collaboration the CardioHealth Alliance was built for. Joining the CardioHealth Alliance will help BridgeBio strengthen the evidence base for turning clinical insight into standard practice." - Jennifer Hodge, PhD, Vice President, Evidence Generation, BridgeBio Established by leaders from the Duke Clinical Research Institute and the Stanford Center for Clinical Research in 2020, the CardioHealth Alliance engages clinicians, data scientists, health care leaders, and policy makers to improve disease care pathways and expedite the implementation of evidence into practice. BridgeBio joins this multidisciplinary group of experts across 13 health systems and five life science partners who are working together to * Use real-world data to inform real-world care * Develop and test new pathways and practices * Scale and optimize best practices * Continuously address value of care through effective policy The Alliance will continue to leverage partnerships with large health systems, academic institutions, and life science partners, including BridgeBio, to manage a broad portfolio of research focused on improving care delivery and outcomes across cardiometabolic conditions. The collaboration aims to address major public health concerns by helping evidence-based therapies and care approaches become integrated into real-world clinical practice. "To accelerate progress in clinical care for people with heart disease, we must embrace a collaborative, cross-disciplinary approach that fosters innovation in how we study health and apply new insights," said Javed Butler, MD, MPH, MBA, Alliance Executive Committee Co-Chair; President, Baylor Scott & White Research Institute; and Senior vice president, Baylor Scott & White Health. "By drawing on the shared expertise of our partners in the CardioHealth Alliance, we can deliver data-informed solutions more quickly to the patients who need them most."