Mid-level associate role in a national life sciences and healthcare regulatory practice. The team advises developers and manufacturers across pharmaceuticals, biologics, devices, diagnostics and related industries on regulatory compliance, investigations, and policy matters.

Work will focus on drug-pricing and fraud & abuse matters, including counseling and litigation-support related to pricing programs and government reimbursement. The group collaborates closely with litigation, transactions and IP teams and provides formal training and mentoring for associates.

At least 3 years of substantive experience with drug pricing and fraud & abuse matters; specific experience with the 340B Program and the Medicaid Drug Rebate Program required
Strong legal research, writing and analytical skills; ability to work independently and in teams
Licensed, or eligible to be licensed, to practice in the jurisdiction(s) of application
Excellent academic credentials and professional references

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