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Regeneron Pharmaceuticals

Develops biopharmaceutical therapies for serious diseases

Director Medical Affairs - Rare Diseases

Full-Time
€125.3k - €208.8k/yr
Senior, Expert
Bachelor's, PharmD, PhD, MD
Munich, Germany
HybridHybrid role in Munich; approximately 30–50% national and international travel required.

About the job

Requirements
  • An MD, DO, PharmD, PhD, or equivalent advanced scientific or clinical degree is required.
  • A minimum of 8 years of Medical Affairs experience with increasing responsibility is required.
  • Expertise in rare diseases and/or genetic medicine is required.
  • Experience leading medical strategy, scientific communications, and evidence generation is required.
  • A strong understanding of drug development and lifecycle management is required.
  • Fluency in English is required.
  • Willingness to travel nationally and internationally approximately 30–50% is required.
Responsibilities
  • Lead medical strategies and tactical plans across assigned rare disease assets and therapeutic areas.
  • Provide scientific and medical leadership throughout pre-launch, launch, and post-launch phases.
  • Establish scientific partnerships with healthcare professionals, researchers, advocacy organisations, payers, and other external stakeholders.
  • Drive evidence generation through Medical Affairs studies, data analysis, publications, and scientific communication plans.
  • Translate clinical and country insights into recommendations supporting medical strategy, patient access, and value demonstration.
  • Manage complex priorities, budgets, and timelines while maintaining scientific integrity and compliance.
Desired Qualifications
  • Experience in rare genetic diseases, gene therapy, regenerative medicine, or rare bone, muscle, or cardiovascular disorders.
  • Product launch, clinical trial, publication, or field Medical Affairs leadership experience.
  • Multi-country experience and additional languages.

About the company

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Regeneron Pharmaceuticals

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Regeneron Pharmaceuticals develops and commercializes medicines for serious diseases, with a focus on cancer, eye diseases, allergic and inflammatory diseases, and infectious diseases. Its products come from using proprietary research capabilities and technologies to discover and develop therapies, often in collaboration with academic, research, and industry partners. Revenue comes from selling approved medicines and from licensing its technologies and entering co-development and co-commercialization partnerships. The company works with healthcare providers and regulators to ensure treatment delivery and safety. Its goal is to improve patient outcomes by bringing life-transforming medicines to market through rigorous R&D and strategic collaborations, maintaining leadership in biopharmaceutical innovation.

Company Size

10,001+

Company Stage

IPO

Headquarters

Town of Mount Pleasant, New York

Founded

1988

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Simplify's Take

What believers are saying

  • Q2 2026 revenue rose 17% to $4.3 billion, with record product sales.
  • Sanofi paid $1 billion upfront on October 1, 2026, validating Regeneron's pipeline.
  • FDA extended EYLEA HD dosing to 20 weeks in April 2026, strengthening retention.

What critics are saying

  • Samsung launches an EYLEA biosimilar in January 2027, pressuring ophthalmology revenue.
  • The May 2026 fianlimab-Libtayo melanoma trial failure triggered an $11 billion selloff.
  • Dupixent patent protections face erosion within five years, inviting biosimilar competition.

What makes Regeneron Pharmaceuticals unique

  • Dupixent and EYLEA HD keep producing category-leading revenue in 2026.
  • Regeneron controls discovery while Sanofi handles global commercial scale on Dupixent.
  • Cemdisiran gives Regeneron a differentiated C5 program with a November 2026 FDA date.

Help us improve and share your feedback! Did you find this helpful?

Benefits

Health Insurance

Wellness Program

Paid Vacation

Equity Awards

Annual Bonuses

Flexible Work Hours

Growth & Insights and Company News

Headcount

6 month growth

↑ 10%

1 year growth

↑ 12%

2 year growth

↑ 12%
Yahoo Finance
Oct 1st, 2026
Sanofi, Regeneron expand alliance in up to $8B deal for immunology drugs

France's Sanofi and US-based Regeneron Pharmaceuticals will expand their 20-year partnership to jointly develop and market immunology medicines in a deal worth up to $8 billion. Regeneron will receive $1 billion upfront, with potential additional payments of up to $7 billion tied to development, regulatory, and commercial targets. The collaboration will add four next-generation immunology drug candidates invented by Regeneron, with one currently in early-stage trials for eczema. The companies will equally share development costs and future profits from new drugs, whilst their existing profit-sharing agreement for top-selling medicine Dupixent remains unchanged. The deal settles prior litigation between the companies and marks an early move by Sanofi's new chief executive Belen Garijo to strengthen the company's pipeline.

Yahoo Finance
Sep 28th, 2026
Regeneron stock down 1% in 2024 despite strong Q2 growth ahead of Q3 earnings on 30 October

Regeneron Pharmaceuticals' stock has declined roughly 1% this year, despite being a strong long-term performer. The biotech company will report third-quarter earnings on 30 October, which could provide a catalyst for the struggling share price. When Regeneron last reported results in July, revenue totalled $4.3 billion, up 17% year-over-year. Global sales of Dupixent and Libtayo rose 38% and 30% respectively, whilst Eylea HD revenue in the US climbed 52%. The strong figures pushed the stock to a new 52-week high in early September. The company has roughly 50 product candidates in development. Regeneron trades at 19 times trailing earnings and less than 15 times forward earnings, compared to the S&P 500's multiples of 23 and 20 respectively.

Investor's Business Daily
Sep 28th, 2026
Why this Regeneron eye rival just catapulted more than 120%.

Why this Regeneron eye rival just catapulted more than 120%. * ALLISON GATLIN * Updated 09:58 AM ET 09/28/2026 Kodiak Sciences (KOD) stock skyrocketed Monday on a double win for its potential rivals to Regeneron Pharmaceuticals' (REGN) blockbuster eye drug, Eylea. Kodiak tested its drugs, Zenkuda and KSI-501, in patients with wet age-related macular degeneration. In this condition, abnormal blood vessels grow under the retina and leak fluid or blood, causing a rapid loss of central vision. Investors Are Rotating Into Healthcare. Here's Why. Janus Henderson portfolio manager Dan Lyons discusses why he sees opportunities for market outperformance in the healthcare sector as innovations in biotechnology, pharmaceuticals and medical devices proliferate. Investors Are Rotating Into Healthcare. Here's Why. See All Videos In the study, both Zenkuda and the earlier-stage drug, KSI-501, proved to be non-inferior to aflibercept after a year of treatment. Aflibercept is the chemical behind Eylea. Kodiak stock soared more than 120% to 72.47 in morning trades. Shares opened at a four-year high. Regeneron stock slipped 2.5% to 768.33. Both drugs show promise. Evercore ISI analyst Umer Raffat says investors only expected a "win" for Zenkuda which, like Eylea, works to block VEGF. VEGF, or anti-vascular endothelial growth factor, is a protein that leads to abnormal blood vessel growth. Eylea uses the same mechanism. But the earlier-stage KSI-501 also showed promise. KSI-501 blocks VEGF and IL-6, an inflammatory protein linked to the development and severity of wet age-related macular degeneration, or wet AMD. Zenkuda showed "meaningful vision gains as well as rapid and sustained retinal drying" for 54% on patients on every-six-months dosing. Zenkuda is given as an injection in the eye. "Today's results are deeply satisfying," Kodiak Chief Medical Officer J. Pablo Velazquez-Martin said in a written statement. "Four years and seven months after our first Phase 3 readout, Zenkuda's profile has come fully into focus through rigorous science, disciplined learning and thoughtful execution." KSI-501, also called tabirafusp alfa tedromer, met the study's vision goal. Kodiak Sciences is starting the Phase 3 study and accelerating enrollment in a study of patients with diabetic macular edema. The company is further planning to ask the Food and Drug Administration to approve Zenkuda in the fourth quarter. Dosing is the 'cherry on top' Raffat called the every-six-months dosing the "cherry on top" for Kodiak Sciences. That company used a strict "treat-to-dry" retreatment criteria. So, for 54% of patients, the results were durable for six months after the injection. The drugs also proved safe and tolerable. But the single most important line in the press release comes from Dr. Charles Wykoff, chairman of research at the Retina Consultants of Texas and a professor of clinical ophthalmology and deputy chair of ophthalmology at the Blanton Eye Institute. Wykoff, Raffat said, "is one of the most prolific retina trialists." "The Zenkuda results exceeded my expectations," Wykoff said. Dr. David Brown, chief medical officer for Retina Consultants of America, said the "holy grail" in treating wet AMD is finding something that delivers "robust anatomic disease control and maximal vision gains, sustained with less frequent dosing." In this way, the results of the study are "truly impressive," he said in a written statement. IBD newsletters. Get exclusive IBD analysis and actionable news daily. Follow Allison Gatlin on X/Twitter at @AGatlin_IBD. YOU MAY ALSO LIKE:

Seeking Alpha
Sep 23rd, 2026
Regeneron Pharmaceuticals, Inc. (REGN) presents at Bernstein Insights: Healthcare Leaders and Disruptors - 3rd Annual Healthcare Forum transcript.

Regeneron Pharmaceuticals, Inc. (REGN) presents at Bernstein Insights: Healthcare Leaders and Disruptors - 3rd Annual Healthcare Forum transcript. 162.3K Followers Regeneron Pharmaceuticals, Inc. (REGN) Bernstein Insights: Healthcare Leaders and Disruptors - 3rd Annual Healthcare Forum September 23, 2026 10:30 AM EDT Company Participants Ryan Crowe - Senior Vice President of Investor Relations & Strategic Analysis Christopher Fenimore - Executive VP of Finance & CFO Conference Call Participants Jeffrey Walch - Bernstein Institutional Services LLC, Research Division Presentation Jeffrey Walch Bernstein Institutional Services LLC, Research Division Thank you so much for our next conversation with health care leaders and disruptors. I have the pleasure of speaking with Regeneron Pharmaceuticals. My name is Jeffrey Walch. I'm one of the analysts at Bernstein, I cover U.S. Biotechnology. And I'm very excited today to talk to 2 of the senior leaders at Regeneron, Chris Fenimore, EVP, Finance and CFO; and Ryan Crowe, SVP, Investor Relations. Before we kick off, I think, Ryan, you have something to read. Ryan Crowe Senior Vice President of Investor Relations & Strategic Analysis I sure do, Jeffrey. Thank you so much for having us. And I'll just briefly read a forward-looking statement reminder that remarks made today may include forward-looking statements about Regeneron, and each forward-looking statement is subject to risks and uncertainties that could cause actual results and events to differ materially from those projected in such statements. A description of material risks and uncertainties can be found in Regeneron's SEC filings. Regeneron does not undertake any obligation to update any forward-looking statements, whether as a result of new information, future events or otherwise. And with that, Jeffrey, why don't we hop into your questions? Question-and-Answer Session Jeffrey Walch Bernstein Institutional Services LLC, Research Division Perfect. Well, thank you once again, both of you for chatting with us today. I'll sort of ask the question and whoever or both of you that would like to answer, feel free to do so. So first off, congrats on

Yahoo Finance
Sep 15th, 2026
Novo Nordisk vs Regeneron: Which healthcare stock to buy in 2026?

Novo Nordisk and Regeneron Pharmaceuticals represent distinct pharmaceutical investment opportunities. Novo Nordisk specialises in metabolic disorders, particularly diabetes and obesity treatments, serving patients in roughly 170 countries with a workforce of about 68,800. In fiscal 2025, Novo Nordisk generated nearly $47.7 billion in revenue, up 6.4% year-over-year, with net income of approximately $15.8 billion. The company's net margin stood at 33.1%, whilst its debt-to-equity ratio was 0.7x. Free cash flow reached nearly $4.5 billion. Regeneron focuses on treatments for eye diseases, cancer, and inflammatory conditions using proprietary technologies. The company maintains strategic partnerships with Sanofi and Bayer. In July 2026, Regeneron expanded its cancer therapy pipeline through collaboration with Telix Pharmaceuticals. Notably, two distributors accounted for roughly 77% of Regeneron's gross product revenue in 2025, creating customer concentration risk.