Practice Area: Life Sciences & Healthcare Regulatory

Position Type: Full-Time

Position Overview

A top-tier regulatory practice is seeking a mid-level associate to join its nationally recognized Life Sciences & Healthcare Regulatory Practice Group across multiple major U.S. offices. The role focuses on providing comprehensive legal counsel across healthcare provider/supplier operations and life sciences product regulations in an interdisciplinary environment alongside litigation, white-collar, transactions, and IP teams.

Key Responsibilities

Healthcare Provider Counsel: Advise academic medical centers, health systems, outpatient providers, digital health companies, and healthcare investors on regulatory compliance, operational matters, and supplier regulations.
Life Sciences Regulatory: Support global pharmaceutical, biotech, medical device, diagnostic, dietary supplement, and cosmetics companies on regulatory strategy and compliance.
Cross-Practice Collaboration: Partner with corporate, transactional, litigation, intellectual property, and white-collar defense groups on regulatory aspects of healthcare and life sciences matters.
Research & Advisory: Conduct complex legal research, draft regulatory submissions, and deliver actionable counsel to clients across the healthcare ecosystem.

Candidate Qualifications

Experience: Minimum of 3+ years of experience in healthcare law, including direct representation of hospitals, health systems, providers, or healthcare suppliers.
Licensure: Currently licensed, or eligible to become licensed, to practice law in the jurisdiction where applying.
Skills: Strong legal research, writing, and analytical skills; creative problem-solving ability; capacity to manage workstreams independently while collaborating effectively in deal and case teams.
Credentials: Excellent academic credentials and professional references.

Compensation & Benefits

Salary Range: $260,000 – $365,000 (Base salary, commensurate with experience)
Bonus: Hours-based bonus eligibility

Competências necessárias

Healthcare provider regulatory counseling (academic medical centers, health systems, outpatient providers)Healthcare supplier regulatory complianceLife sciences product regulatory strategy (pharmaceuticals, biotech, medical devices, diagnostics, dietary supplements, cosmetics)Drafting regulatory submissionsComplex legal researchLegal writing (including advisory memoranda and submissions)Legal analysis and interpretation of healthcare/life sciences regulationsCreative problem-solving in regulatory contextsIndependent workstream/project managementCross-practice collaboration and interdisciplinary coordination (corporate, litigation, IP, white-collar teams)Client counseling and delivering actionable regulatory adviceDirect representation of hospitals, health systems, providers, or healthcare suppliersBar licensure or eligibility to practice law in the applying jurisdiction

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