Intern, Regulatory Research
Position Overview
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.
Key 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
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.
Key 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