Mid-level associate role in a national life sciences and healthcare regulatory practice focused on drug pricing, fraud-and-abuse, and related counseling and enforcement matters. The team advises a broad range of life sciences entities, including pharmaceutical, biotech, medical device, diagnostic, and related organizations, on regulatory strategy, investigations, and policy developments.

Day-to-day work includes counseling clients on drug pricing programs and government program compliance, supporting investigations and litigation, and contributing to regulatory comments and policy analysis. The practice collaborates with litigators, transactional teams, and IP colleagues, offering exposure to interdisciplinary matters.

The firm provides substantive training and mentoring, with opportunities to take on high-profile, precedent-setting matters. Applicants must be licensed — or eligible for licensure — in the jurisdiction(s) where they will work.

Minimum 3 years' substantive experience in life sciences regulatory matters, with required experience in drug pricing (including 340B and Medicaid Drug Rebate Program).
Experience advising on fraud-and-abuse and government program compliance matters.
Strong legal research, writing and analytical skills and ability to work both independently and as part of a team.
Excellent academic credentials and references; admitted or eligible for admission to the relevant state bar(s).

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