Life Sciences & Healthcare Regulatory Associate (Mid-Level)

J&T Business Consulting; Denver (CO); On-site; USD 260,000 - 365,000; Full time

Job summary

J&T Business Consulting seeks a Life Sciences & Healthcare Regulatory Associate (Mid-Level) for Denver and other major U.S. offices.

The role provides regulatory counsel across healthcare provider and life sciences product regulations within an interdisciplinary environment alongside litigation, IP, and transactions teams. The ideal candidate has 3+ years in healthcare law, is licensed or eligible to become licensed, and demonstrates strong research, writing, and analytical skills with the

Qualifications

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

Responsibilities

• Advise healthcare providers and suppliers on regulatory compliance and operations.
• Support regulatory strategy for life sciences products across regulators.
• Collaborate with corporate, transactional, litigation, IP, and white-collar defense groups on regulatory matters.
• Conduct complex legal research and draft regulatory submissions, delivering actionable counsel to clients.

Skills

Legal research

Legal writing

Analytical skills

Independent work

Job description

Life Sciences & Healthcare Regulatory Associate (Mid-Level)

Denver, United States | Posted on 11/05/2026

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.

Salary Range: $260,000 – $365,000 (Base salary, commensurate with experience)