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Intern, Regulatory Research

Remote Worldwide Hiring now

Position Overview

This internship will support the curation and research team in identifying, reviewing, and synthesizing clinical and regulatory literature that informs reputed company’s content development pipeline. This role is ideal for reputed company with a background in health sciences who are interested in working with medical literature, clinical standards, and reputed company 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 reputed company documents reputed company 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
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