Intern, Regulatory Research

HEALTHSTREAM INC • Nashville, TN

6d • Remote

About The Position

This internship will support the curation and research team in identifying, reviewing, and synthesizing clinical and regulatory literature that informs HealthStream’s content development pipeline. This role is ideal for students with a background in health sciences who are interested in working with medical literature, clinical standards, and healthcare workforce competency frameworks. The intern will contribute to evidence-informed content development by conducting structured literature searches, reviewing clinical and regulatory guidance, and supporting accuracy and synthesis efforts across research and content teams.

Requirements

• Strong analytical and critical thinking skills, particularly in interpreting clinical and regulatory information
• Excellent written communication skills, with the ability to clearly summarize complex material
• High attention to detail and commitment to accuracy
• Ability to organize and manage information across multiple sources
• Self-directed, proactive, and comfortable working in a remote or hybrid environment

Nice To Haves

• Academic background in neuroscience, pre-med, public health, biology, or related health sciences field
• Familiarity with or strong interest in clinical literature, evidence-based practice, and healthcare standards
• Exposure to or willingness to learn medical and regulatory databases (e.g., PubMed, Federal Register)
• Foundational understanding of clinical research concepts and healthcare delivery environments

Responsibilities

• Conduct structured searches across medical and regulatory databases (e.g., PubMed, Federal Register, state health agency repositories) to identify evidence supporting training content development
• Review and summarize clinical guidelines, evidence-based practice standards, and regulatory updates relevant to assigned care settings
• Assist in tagging, organizing, and maintaining regulatory source documents within internal research repositories
• Support accuracy review of clinical content drafts against primary regulatory and clinical sources
• Contribute to literature synthesis summaries and research memos used by content and product teams

What This Job Offers

• Job Type: Full-time
• Career Level: Intern
• Education Level: No Education Listed