Regeneron Pharmaceuticals, Inc (USA) Posted October 13, 2026

Senior Medical Director, Clinical Development, MASH

Tarrytown, United States Full time
Notify me about similar jobs

Regeneron Pharmaceuticals, Inc (USA) is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Build our future together:

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Medical Director, Clinical Sciences, MASH to join our Genetic Medicines clinical development team. In this role, you will lead one or more MASH clinical programs from first-in-human through registration-enabling studies while collaborating with research, the Regeneron Genetics Center, regulatory affairs, clinical operations, and other partners. Evolving Genetic Medicines modalities include RNA interference (RNAi), gene editing, viral vector gene delivery, and others. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

When & where:

Location: Tarrytown, NY

Discover your role:

Lead one or more MASH clinical programs and serve as the clinical expert with regulators, key opinion leaders, and advisory boards

Design and execute innovative Phase 1, 2, and 3 studies, from first-in-human through registration-enabling

Develop clinical strategies that shorten development timelines in an evolving regulatory landscape

Partner with discovery scientists and translational geneticists to evaluate emerging genetic medicines targets and shape clinical experiments

Provide input to research teams on the next generation of targets in metabolic diseases

Safeguard patient safety in clinical studies and review post-marketing signals alongside Global Patient Safety

Ensure the quality of clinical documents and prepare responses to regulatory agency questions and submissions

Build consensus across matrixed, multi-disciplinary teams and serve as a clinical role model

This role requires:

M.D., D.O., or equivalent medical degree and relevant specialized fellowship/residency training (MD/PhD preferred)

Minimum of 3-4 years of industry clinical development experience with a track record of conducting clinical trials and/or leading clinical programs

Solid knowledge of compliance and global regulatory requirements (ICH) for pharmaceutical development

Strong understanding of operational aspects of all phases of clinical trial conduct (start-up, conduct, close-out)

Experience leading cross-functional or similarly diverse teams

Excellent interpersonal and stakeholder management skills

Preferred: Clinical development experience in MASH

Preferred: Research experience in an academic setting

#MDJOBSCD, #MDJOBS

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all  qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Where necessary, we disclose salary ranges for roles in all countries in which we operate.  The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits.  Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/ . For other locations, additional information will be provided during the recruitment process.  If you have any questions, please speak with your recruiter.

Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.

As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.

For jobs in Canada: this posting is for an existing position.

Salary Range (annually)

$333,300.00 - $450,900.00

Job details

Seniority
Director
Function
Clinical Development
Therapeutic area
Not listed
Location
Tarrytown, United States
Employment type
Full time

How this role compares

Computed from every other active Clinical Development role in our database, not just this employer's listings.

We currently track 339 comparable Director Clinical Development roles across 57 biopharma companies.

339Comparable roles tracked
318Currently active
57Companies hiring similar roles
18Countries represented

Salary context

172 of 339 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject $333,300/yr – $450,900/yr
Lowest disclosed · Patient Safety, Medical Director · Vertex Pharmaceuticals Inc (US) $0/hr – $0/hr (≈ $0–$0/yr)
Peer group range $0 – $392,100 (median $264,000)

Where these roles are based

Top locations among the 339 comparable roles

United States270
United Kingdom22
Switzerland9
India8
Spain6
China4

+ 12 more countries

Seniority mix

339 of 339 peers have a known seniority level

Director241
Senior Director54
Principal44

Therapeutic area mix

100 of 339 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology59
Neuroscience9
Immunology8
Cardiovascular / CVRM8
Respiratory6
Ophthalmology3
Dermatology & Aesthetics3
Vaccines & Infectious Disease3
Rare Disease1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
AstraZeneca Gaithersburg, Maryland, United States of America Director
Same function Same seniority Same country
60%similar
AstraZeneca Gaithersburg, Maryland, United States of America Director
Same function Same seniority Same country
60%similar
AbbVie North Chicago, IL Director
Same function Same seniority Same country
60%similar
AbbVie North Chicago, IL Director
Same function Same seniority Same country
60%similar
AbbVie North Chicago, IL Director
Same function Same seniority Same country
60%similar
AbbVie Director
Same function Same seniority Same country

Open in 2 locations

Waltham, United StatesSouth San Francisco, United States

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

Or follow a whole field: get every new Medical Director job in the United States, and choose locations and companies.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
Global Development Medical Director, Late Respiratory and Immunology Clinical Development
AstraZeneca · Gaithersburg, Maryland, United States of America · Director
Function Therapeutic area Seniority Country
60%
Medical Director/Senior Medical Director, Immunology Clinical Development - Dermatology
AbbVie · North Chicago, IL · Director
Function Therapeutic area Seniority Country
60%
Director, Clinical Pharmacology (Immunology)
AbbVie · Waltham, MA · Director
Function Therapeutic area Seniority Country
60%
Director, Global Clinical Physician (Cardiovascular)
E.R. Squibb & Sons,L.L.C. · Cambridge Crossing, United States · Director
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.