Senior Director, Legal, Corporate Counsel, Market Access (Biotech)

Location: San Rafael and Novato, California, United States

Company

hirify.global is a biotechnology company developing therapies for genetically defined rare diseases.

What you will do

• Provide legal advice to the Market Access organization across pricing, reimbursement, value, evidence, government pricing, patient support, and related commercial activities.
• Advise on Medicaid, Medicare, 340B, Veterans Health Care Act requirements, anti-kickback rules, pricing transparency, and other US healthcare laws.
• Support the development, negotiation, interpretation, and administration of contracts with payers, PBMs, GPOs, specialty pharmacies, distributors, wholesalers, health systems, and patient support vendors.
• Draft and negotiate rebate, value-based, outcomes-based, distribution, data licensing, administrative services, and patient support agreements.
• Review product labeling, promotional and comparative claims, health economic information, scientific exchange materials, and communications regarding clinical data.
• Collaborate with Legal, Compliance, Medical Legal Review, and cross-functional business partners on strategic initiatives and department projects.

Requirements

• Juris Doctor degree from an ABA-accredited law school and membership in a state bar.
• At least 8 years of post-JD experience advising life sciences or biopharmaceutical organizations.
• Experience with government price reporting and pharmaceutical customer contracting across commercial and government stakeholders.
• Experience drafting, reviewing, negotiating, and advising on complex market access, rebate, distribution, data, patient support, and value-based contracts.
• Strong knowledge of Medicaid, 340B, Veterans Administration requirements, anti-kickback statutes, state drug pricing transparency laws, OIG guidance, the False Claims Act, and the PhRMA Code.
• Ability to work at the San Rafael or Novato, California location.

Nice to have

• Experience with health economic and outcomes research, value communications, and market access promotional considerations.
• Experience advising on specialty medicines.

Culture & Benefits

• Collaborative, cross-functional work with Legal, Compliance, Medical, and commercial teams.
• Work in a highly regulated biotechnology environment focused on rare disease therapies.
• Opportunities to contribute to department committees, pro bono initiatives, and community programs.
• Fast-paced environment emphasizing integrity, ethics, practical advice, and business understanding.