BioMarin Pharmaceutical Inc. Posted June 18, 2026

Senior Director, Legal, Corporate Counsel, Market Access

San Rafael, United States Fulltime-Regular
Market Access Senior Director
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BioMarin Pharmaceutical Inc. 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

<p>Who We Are <br /><br />BioMarin is a leading rare disease biotechnology company focused on genetically defined conditions.<br /><br />Guided by our purpose to develop medicines that make a profound impact on people’s lives, our global teams have delivered a portfolio of therapies since our founding in 1997. Our revolutionary treatments for conditions like achondroplasia (the most common form of dwarfism), PKU (phenylketonuria), CLN2, a form of Batten disease, and a number of forms of MPS (mucopolysaccharidosis) offer new possibilities for patients and families who previously had few, if any, available options. More recently, with the close of the Amicus acquisition, our portfolio has expanded to include therapies for Fabry disease and Pompe disease, expanding our ability to reach more people living with rare genetic conditions.<br /><br />Our success comes from our unwavering commitment to excellence, our deep understanding of patient needs, our scientific expertise, and our world-class manufacturing capabilities. At the heart of BioMarin is a dedicated team of the brightest minds in the industry working together to deliver innovative therapies to patients and families around the world. <br /><br />About Corporate Groups <br /><br />It takes a village, and at BioMarin, our general and admin teams are the village behind our success. From the IT experts who manage our technology to the human resources professionals who hire the people who make it all possible, these teams support our organization and span all areas of operations.</p><div style="line-height: normal;">This role provides expert Legal advice to the business on a wide range of activities within a highly regulated environment. This role is responsible for providing legal support to the Market Access function within BioMarin, including Pricing, Access, Value, and Evidence which supports, Managed Markets, Pricing, Government Pricing, Patient Support and related functions. The ideal candidate will have prior experience counseling prescription drug companies on legal issues relating to market access, government pricing, contracting, federal and state laws impacting pricing and access, antitrust, state pricing transparency patient assistance, brand strategy and product commercialization activities.</div><div><b><u>Key Responsibilities</u></b></div><ul style="margin-top: 0.0px;"><li>Advise business partners on various Commercial initiatives in a way that advances the company’s strategy while addressing legal risks and protecting the company’s integrity and reputation</li><li>Provide legal advice and counsel on:</li><ul style="margin-top: 0.0px;"><li>Statutory and regulatory obligations under Medicaid, Medicare, 340B program, Veterans Health Care Act</li><li>Market access and reimbursement issues</li><li>Government pricing, including price reporting compliance policies and reasonable assumptions documents</li><li>Centers for Medicare and Medicaid final rules and correspondence including letters and public comments on proposed rules and guidance</li><li>Proposed and enacted United States federal and state legislation impacting pharmaceutical companies relating to market access, pricing, reimbursement as well as state drug price reporting and transparency laws and compliance</li><li>Services and contracting relating to specialty distributors and specialty pharmacies</li><li>Data and special projects</li><li>Brand strategic planning and business operation plans</li><li>Staying abreast of evolving healthcare legislation and regulations and the enforcement landscape</li></ul><li>Provide legal counsel and strategic support for the development, negotiation, interpretation, and administration of a broad range of pharmaceutical commercial contracts and arrangements with customers including:</li><ul style="margin-top: 0.0px;"><li>Commercial and government payers</li><li>Pharmacy Benefit Managers (PBMs)</li><li>Group Purchasing Organizations (GPOs)</li><li>Specialty pharmacies and distributors</li><li>Wholesalers and distribution partners</li><li>Integrated Delivery Networks (IDNs)</li><li>Health systems and provider organizations</li><li>Patient support and patient services vendors</li></ul><li>Review, draft, and negotiate rebate agreements, value-based and outcomes-based agreements, administrative service agreements, distribution agreements, data licensing agreements, patient support agreements, and other market access-related contracts.</li><li>Ensure compliance with applicable laws and company policies, including Anti-kickback Statute and other US healthcare compliance laws and regulations</li><li>Collaborate with Legal and Compliance colleagues to ensure delivery of comprehensive legal advice</li><li>Participate in Medical Legal Review to provide guidance regarding external messaging</li><li>Review and counsel on product labeling, promotional claims, comparative claims, health economic information, scientific exchange activities, and communications regarding clinical data, as necessary</li><li>Contribute to the Legal & Compliance Department</li><li>Participate in various Legal & Compliance Department projects and initiatives, including committees such as Culture and Pro Bono & Community</li><li>Share information and knowledge through group presentations and individual discussions with peers and managers</li></ul><div>Qualifications, Professional Skills, and Preferred Experience</div><ul style="margin-top: 0.0px;"><li>JD from an ABA accredited law school</li><li>Member of a state bar</li><li>Minimum of 8 years post-JD experience advising on legal matters in a life sciences space, whether in a law firm or in-house in the biopharmaceutical industry, or both</li><li>Government price reporting experience</li><li>Familiarity with health economic and outcomes research (HEOR), value communications, and market access promotional considerations is preferred.</li><li>Strong ability to provide practical, business-oriented legal advice in a highly regulated environment while balancing legal, regulatory, reputational, and commercial considerations.</li><li>Experience advising on statutes, regulations, and guidance documents applicable to market access activities, including Medicaid, 340B program, Veterans Administration, federal and state anti-kickback statutes, state drug pricing transparency laws, OIG guidance documents and advisory opinions, the False Claims Act, and the PhRMA Code</li><li>Significant experience advising on pharmaceutical customer contracting across a broad range of stakeholders, including commercial and government payers, Pharmacy Benefit Managers (PBMs), Group Purchasing Organizations (GPOs), specialty pharmacies, specialty distributors, wholesalers, Integrated Delivery Networks (IDNs), and healthcare providers.</li><li>Demonstrated experience drafting, reviewing, negotiating, and counseling on complex market access, rebate, distribution, administrative services, data, patient support, and value-based contracting arrangements.</li><li>Outstanding ability to effectively communicate (verbally and in writing), sound legal advice to lawyers and non-lawyers alike, coupled with a strong understanding of business needs</li><li>Excellent analytical, problem-solving and organizational skills to handle multiple responsibilities simultaneously and still meet high quality and timeliness standards</li><li>Ability to effectively and efficiently manage outside counsel and adhere to a budget</li><li>Experience providing legal advice on specialty medicines is highly desired</li><li>Enjoys working collaboratively and cross-functionally on teams, as well as independently</li><li>Proactively solves problems and makes decisions with integrity and ethics</li><li>Thrives in a fast-paced and dynamic environment</li><li>Is eager to take on new challenges</li></ul><p><br /><br /><br />Note: This description is not intended to be all-inclusive, or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned. <br /><br />Equal Opportunity Employer/Veterans/Disabled <br /><br />An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.</p>

Job details

Seniority
Senior Director
Function
Market Access
Therapeutic area
Not listed
Location
San Rafael, United States
Employment type
Fulltime-Regular

How this role compares

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

We currently track 56 comparable Senior Director Market Access roles across 27 biopharma companies.

56Comparable roles tracked
52Currently active
27Companies hiring similar roles
12Countries represented

Salary context

15 of 56 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 Not listed on this posting
Peer group range $223,450 – $290,000 (median $244,150)

Where these roles are based

Top locations among the 56 comparable roles

United States32
United Kingdom5
Germany4
Ireland4
Switzerland3
France2

+ 6 more countries

Seniority mix

56 of 56 peers have a known seniority level

Director46
Senior Director8
Executive/VP2

Therapeutic area mix

25 of 56 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Immunology8
Neuroscience6
Rare Disease6
Oncology3
Dermatology & Aesthetics2

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.

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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.

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%
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Function Therapeutic area Seniority Country
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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.