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We are currently seeking experienced Market Access Lawyers  to work with leading pharmaceutical companies. Responsibilities Provide proactive, business‑oriented legal and compliance advice on  market access, pricing, and reimbursement  strategies for pharmaceutical and biologic products. Advise on  government pricing and reporting  (e.g., Medicaid Best Price, AMP, ASP, 340B, VA/FSS) and the impact of commercial contracting strategies on those obligations. Support  coverage, coding, and reimbursement  initiatives with market access, HEOR, trade/channel, and pricing teams. Draft, review, negotiate, and advise on a broad range of  market access–related agreements , including: PBM, payer, and GPO agreements Wholesaler, specialty pharmacy, and distribution agreements Discount, rebate, and value‑based/outcomes‑based contracts Consulting, advisory board, master services, and data‑sharing agreements related to market access activities Counsel on the design and implementation of  patient support programs , co‑pay assistance, and related arrangements, with attention to anti‑kickback and False Claims Act risk. Partner with commercial, medical, regulatory, and compliance teams to ensure that  access‑related strategies, communications, and materials  comply with applicable laws, regulations, and industry codes. Stay current on  U.S. federal and state laws, regulations, and enforcement trends  impacting market access, pricing, reimbursement, and interactions with payers, PBMs, and health care professionals. Minimum Qualifications 5–8 years of experience as an attorney in a law firm and/or in‑house with a  pharmaceutical or biopharmaceutical company , with a significant focus on  market access, pricing, reimbursement, and/or government price reporting . Experience drafting and negotiating  PBM, payer, GPO, wholesaler, rebate, and other market access–related agreements . Prior experience counseling on legal issues relating to  advertising and promotion, scientific exchange, patient support programs, and interactions with health care professionals and payers . Strong knowledge of, and experience advising on, statutes, regulations, and guidance applicable to commercial and market access activities, including: FDCA and FDA regulations and guidance Federal and state anti‑kickback statutes and beneficiary inducement rules OIG guidance documents and advisory opinions False Claims Act PhRMA Code and relevant industry standards Demonstrated ability to  translate complex regulatory requirements into practical, risk‑based contracting and access strategies . Efficient multitasker with strong interpersonal and communication skills; able to work independently and  cross‑functionally  with market access, commercial, medical, regulatory, compliance, and finance teams. Positive, solutions‑oriented mentality and willingness to tackle new and evolving business needs in a fast‑paced environment. Licensed and in good standing to practice law in your state of primary residence.   Compensation:   The estimated total compensation for full-time Axiom attorney roles is $104,500-325,000 per year and for non-attorney roles is $71,250-309,750 per year.   Compensation decisions are based on various factors, including, but not limited to, experience, skills, certifications, location, and business needs.  Employees may be eligible for additional benefits, including health, dental, and vision insurance; paid holidays and PTO; flexible work arrangements; and professional development opportunities and tools.   About Axiom:   For over 25 years, Axiom has pioneered the alternative legal services industry, now serving more than 1,500 legal departments globally with our unique blend of