Regeneron Pharmaceuticals, Inc (USA) Posted July 31, 2026

Senior Director, Patient Advocacy

Sleepy Hollow, United States Full time
Regulatory Affairs Senior Director

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're looking for a Senior Director, Patient Advocacy to join our Patient Advocacy team, shaping enterprise-wide strategy across discovery, development, and commercialization from our Sleepy Hollow, NY campus. In this role, you'll build the operating model that brings the patient voice into executive decision-making, partnering closely with Medical, Commercial, Market Access, Policy, and Clinical Development. This position offers the opportunity to shape how a fast-growing, science-driven organization listens to and acts on patient needs, making a meaningful difference for people living with serious diseases worldwide.

When & where:

Location: Sleepy Hollow, NY

Work model/flexibility: Hybrid, onsite 4 days per week

Discover your role:

Shape Regeneron’s enterprise-wide patient advocacy strategy, connecting the patient voice to discovery, development, and commercialization.

Build the standards and governance that guide how we engage advocacy and professional organizations.

Partner with Medical, Commercial, Market Access, Policy, and Clinical Development to set a multi-year advocacy roadmap.

Drive measurable outcomes, faster diagnosis, stronger trial awareness, broader access, and a better patient experience.

Move fluidly between big-picture strategy and hands-on execution, leading through influence across teams.

Turn corporate priorities into focused, therapeutic-area plans with clear decision rights.

Read external trends and policy shifts early, and recommend the moves that keep patient impact and business goals aligned.

Report progress through KPIs, dashboards, and board-ready materials that keep senior leaders informed.

This role might be for you if:

You've built enterprise-level programs from the ground up and know how to earn buy-in across an organization.

You're comfortable being a visible advisor to senior leaders and advocacy partners alike.

You bring structure to ambiguity, turning broad strategy into clear, repeatable processes.

You communicate with precision, able to distill complex work into a concise, data-driven story.

You’ve partnered across Medical, Commercial, Market Access, and Policy functions and understand the compliance considerations that come with advocacy work.

You put patients first, and let that perspective shape decisions, budgets, and partnerships.

You're energized by leading through influence rather than direct authority.

This role requires:

Bachelor's degree and 12+ years of relevant experience, including 10+ years leading multi-stakeholder patient advocacy programs

A track record of building enterprise-wide, cross-functional programs with visible business impact

Strong executive presence and communication skills, with experience preparing board-ready materials

Experience partnering with Medical, Commercial, Market Access, and Policy teams, with working knowledge of compliance in advocacy

Preferred: experience in rare disease, oncology, hematology, ophthalmology, immunology, or cardio-metabolic disease

Preferred: experience operating in complex, matrixed, or global organizations; alliance management experience is a plus

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)

$216,100.00 - $360,200.00

Job details

Seniority
Senior Director
Function
Regulatory Affairs
Therapeutic area
Not listed
Location
Sleepy Hollow, United States
Employment type
Full time

How this role compares

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

We currently track 83 comparable Senior Director Regulatory Affairs roles across 24 biopharma companies.

83Comparable roles tracked
66Currently active
24Companies hiring similar roles
10Countries represented

Salary context

36 of 83 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 $216,100/yr – $360,200/yr
Peer group range $174,000 – $380,750 (median $245,550)

Where these roles are based

Top locations among the 83 comparable roles

United States53
Ireland9
United Kingdom8
Poland4
Spain3
China's Mainland2

+ 4 more countries

Seniority mix

83 of 83 peers have a known seniority level

Director61
Senior Director11
Executive/VP11

Therapeutic area mix

10 of 83 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology3
Cardiovascular / CVRM2
Rare Disease2
Respiratory2
Neuroscience1

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
Lilly Indianapolis, Indiana, United States of America Senior Director
Same function Same seniority Same country
60%similar
Lilly Indianapolis, Indiana, United States of America Senior Director
Same function Same seniority Same country
60%similar
E.R. Squibb & Sons,L.L.C. New Brunswick, United States Senior Director
Same function Same seniority Same country
60%similar
E.R. Squibb & Sons,L.L.C. Princeton, United States Senior Director
Same function Same seniority Same country
60%similar
E.R. Squibb & Sons,L.L.C. Princeton, United States Senior Director
Same function Same seniority Same country
60%similar
GlaxoSmithKline LLC Upper Providence, United States Senior Director
Same function Same seniority Same country

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%
Senior Director - Global Regulatory Affairs - Global Regulatory Lead, Regulatory Strategy
Lilly · Indianapolis, Indiana, United States of America · Senior Director
Function Therapeutic area Seniority Country
60%
Senior Director, Global Scientific and Regulatory Documentation, Content Strategy
E.R. Squibb & Sons,L.L.C. · Princeton, United States · Senior Director
Function Therapeutic area Seniority Country
60%
Regulatory Affairs Senior Director - Global Regulatory Leader - Oncology
Amgen Inc. · Remote, United States · Senior Director
Function Therapeutic area Seniority Country
50%
Director, RA Global Regulatory Strategy
AbbVie · North Chicago, IL · Director
Function Therapeutic area Adjacent 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.