Genzyme Corporation Posted September 1, 2026

HEVA Business Partner

Cambridge, United States Full time
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Genzyme Corporation 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

Job title:  HEVA (HEOR) Business Partner

Location: Cambridge, MA or Morristown, NJ (hybrid with 3 days a week on-site requirement)

About the Job

At Sanofi, we chase the miracles of science to improve people's lives. As a global pharmaceutical leader, we are committed to transforming the practice of medicine by working to turn the impossible into the possible. Our mission drives us to pursue breakthrough therapies and innovative solutions that address the world's most challenging health conditions. We believe that when we bring together diverse perspectives, cutting-edge science, and unwavering dedication to patients, we can achieve extraordinary outcomes that make a meaningful difference in the lives of millions worldwide.

Sanofi's Rare franchise has a diverse and fast-growing portfolio. This includes late-stage launching candidates as well as several promising compounds in the pipeline. HEVA's mission is to conduct, communicate, and translate evidence to demonstrate the value of Sanofi's products and support optimal access and treatment outcomes for patients.

HEVA Vision, Mission, and Values

We are one bold HEOR team leveraging innovative HEOR to transform patient care and access. As HEOR experts, we lead the generation and dissemination of robust, business-relevant evidence to demonstrate value and drive access to medicines. The HEVA organization is driven by five core values that define how we work and deliver impact. We operate as One Team, partnering without boundaries while pursuing a Bold Purpose through ambitious, measurable goals. Grounded in Scientific Excellence with Relevance and deep technical expertise, we embrace Innovation in Action to transform how we research and deliver Impact for People, creating meaningful outcomes for patients, the healthcare ecosystem, and our colleagues who make it all possible.

Join the team transforming care for people with immune challenges, rare diseases, cancers, and Specialty Care neurological conditions. In Specialty Care, you’ll help deliver breakthrough treatments that bring hope to patients with some of the highest unmet needs.

About Sanofi

We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.

Main Responsibilities

This role will lead Health Economic and Outcomes Research activities for AYVAKIT® in Systemic Mastocytosis and emerging pipeline assets within the Global Rare HEVA team.

Lead the development and execution of asset‑level HEOR strategies within the global HEVA framework for AYVAKIT® (avapritinib) in Systemic Mastocytosis (advanced SM and indolent SM) and assigned emerging pipeline assets, translating Target Value Propositions and access strategies into evidence hypotheses, requirements, and generation plans that address payer/provider/health system unmet needs in rare mast cell disease; operate with medium independence for strategic work and high independence for tactical execution.

Design and execute HEOR research, including economic modeling, database analysis, observational research, Clinical Outcomes Assessment (COA) development and validation, systematic literature review, evidence synthesis, and value dossier development, and operationalize and execute evidence generation priorities for assigned Systemic Mastocytosis indications and emerging assets, incorporating them into broader Sanofi planning documents such as the Integrated Evidence Generation Plan (IEGP).

Operate as part of a multi-functional global brand and development team responsible for designing clinical research programs to meet the evidentiary standards of regulators, HTA organizations, reimbursement authorities, and third-party payers; provide trial design recommendations; serve as a subject matter expert providing input to commercial, medical, market access, and strategy development teams; and align closely with the US HEVA team to ensure the global evidence strategy reflects US access and payer needs.

Develop collaborative research relationships with payers and other decision-makers to inform value demonstration strategies for AYVAKIT® and pipeline assets, leveraging payer interactions to identify strategies that improve the impact of research and build advocates for data; support interactions with global HTA bodies and reimbursement authorities; and engage with key opinion leaders and external research partners to advance HEVA science in Systemic Mastocytosis.

Contribute to scientific publications and presentations in peer-reviewed journals and at major congresses; distill complex HEOR findings into clear, audience-appropriate communications for internal and external stakeholders; maintain compliance with all relevant internal SOPs and external laws and regulations; and mentor junior colleagues on a case-by-case basis, sharing HEOR expertise and supporting their professional development.

About You

Advanced degree (PhD, MD, MS, MPH, or PharmD) in a scientific discipline

5 years of experience in health economics, outcomes research, or a related field

Global product launch experience; understanding of payer evidence requirements and value demonstration in a competitive market

Demonstrated experience applying various HEOR methods to specific research projects and supporting global launches

Proficiency in principles of evidence-based medicine and clinical research methodology, economic modeling, and COAs

Experience in translating Target Value Propositions and access strategies into evidence hypotheses, requirements, and generation plans

Established track record of scientific and/or methods publications in peer-reviewed journals

Knowledge of global HTA processes and guidelines; experience with HTA submissions preferred

Strong ability to partner with colleagues from non-HEOR functional areas

Compliance with all relevant internal SOPs and external laws and regulations

Technical Skills:

Demonstrated understanding of disease physiopathology, drug mechanism of action, health economic modeling, clinical development principles, epidemiology, biostatistics, statistical programming, COA development, systematic literature reviews, and network meta-analyses

Working proficiency with HEOR-relevant digital tools and data platforms; ability to apply digital solutions to enhance research efficiency

Soft Skills:

Strong communication skills, both verbal and written, including presentation skills; significant experience making presentations to senior management strongly desired

Understanding of the legal and regulatory environment of the pharmaceutical industry; demonstrated integrity on compliance considerations and solid ethics

Entrepreneurial spirit, team orientation, and ability to develop creative solutions to complex problems

Why Choose Us?

Bring the miracles of science to life alongside a supportive, future-focused team.

Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.

Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.

Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.

Sanofi Inc. and its U.S. affiliates are Equal Opportunity employers committed to a culturally inclusive workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.

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Pursue progress , discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

Sanofi US endeavours to make our career center accessible to any and all users. If you are experiencing difficulty and need assistance applying online, please call 1-866-SANOFI2 (1-866-726-6342) or click here

US and Puerto Rico Residents Only

Sanofi Inc. and its U.S. affiliates are Equal Opportunity employers committed to a culturally inclusive workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.

North America Applicants Only

The salary range for this position is:

$178,500.00 - $257,833.33

All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can  be found here.

Job details

Seniority
Not listed
Function
Market Access
Therapeutic area
Not listed
Location
Cambridge, United States
Employment type
Full time

How this role compares

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

We currently track 249 comparable Market Access roles across 58 biopharma companies.

249Comparable roles tracked
226Currently active
58Companies hiring similar roles
42Countries represented

Salary context

59 of 249 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject $178,500/yr – $257,833/yr
Peer group range $75,510 – $290,000 (median $187,600)

Where these roles are based

Top locations among the 249 comparable roles

United States104
India17
China12
Germany11
United Kingdom10
Japan8

+ 36 more countries

Seniority mix

192 of 249 peers have a known seniority level

Manager93
Director46
Associate Director31
Senior Director9
Senior6
Intern/Fellow/Postdoc5
Executive/VP2

Therapeutic area mix

61 of 249 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Neuroscience24
Oncology14
Immunology10
Rare Disease7
Dermatology & Aesthetics4
Ophthalmology2

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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.

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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.