Life Sciences & Healthcare Regulatory Associate (Mid-Level)

J T; San Francisco (CA); Sur place; USD 260 000 - 365 000; Plein temps

Résumé du poste

J T in the United States seeks a mid-level associate for its Life Sciences & Healthcare Regulatory Practice Group. The role focuses on regulatory compliance for healthcare providers and life sciences products, working across offices and collaborating with litigation, IP, and transactional teams.

Requirements include 3+ years in healthcare law, active or eligible bar licensure, strong research and writing skills, and the ability to manage workstreams while coordinating with cross-functional teams.

Qualifications

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

Responsabilités

• Advise academic medical centers, health systems, providers, and healthcare suppliers on regulatory compliance and provider regulations.
• Support global life sciences regulatory strategy for pharmaceutical, biotech, medical device, diagnostic, dietary supplement, and cosmetics companies.
• Collaborate with corporate, transactional, litigation, IP, and white-collar defense groups on regulatory aspects of healthcare and life sciences matters.
• Conduct complex legal research, draft regulatory submissions, and deliver actionable counsel to clients across the healthcare ecosystem.

Connaissances

Legal research

Legal writing

Analytical skills

Project management

Collaborative skills

Formation

Juris Doctor (JD)

Description du poste

Locations: Boston, MA | Chicago, IL | Denver, CO | Los Angeles, CA | New York, NY | San Francisco, CA | Seattle, WA | Silicon Valley, CA | Washington, DC

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