CLINCAL RESEARCH APPRENTICE

Duke CareersDurham, NC
$21 - $31Onsite

About The Position

The Clinical Research Unit at Duke University is looking for a Clinical Research Apprentice to join our team. This is an exciting opportunity to launch your clinical research career through a full-time apprenticeship supported by Bloomberg Philanthropies. In this role, you will gain hands-on experience while learning directly from experienced Clinical Research Professionals and building foundational skills in clinical trials, participant engagement, data management, and research operations. You will work alongside research teams supporting studies across a variety of clinical research domains while completing work-based learning experiences designed to increase your knowledge, confidence, and independence over time. This role is ideal for someone passionate about healthcare, research, and improving patient outcomes through clinical discovery.

Requirements

  • Associate’s degree in Clinical Research or successful completion of the approved Clinical Research Pre-Apprenticeship program
  • Completion of the Durham Technical Community College Clinical Trials Research Associate’s Degree training is required as a pre-requisite of the apprenticeship
  • Ability to use standard computing software and web-based applications, including Microsoft Office products
  • Strong communication and organizational skills
  • Ability to work collaboratively in a team-based environment
  • Interest in clinical research and participant-centered care

Nice To Haves

  • Prior exposure to healthcare or clinical environments
  • Familiarity with electronic health records (EHR) or research databases
  • Demonstrated attention to detail and ability to follow standard operating procedures
  • Interest in learning Good Clinical Practice (GCP) and regulatory requirements

Responsibilities

  • Perform clinical research tasks under supervision while increasing independence over time
  • Assist with study participant screening, recruitment, scheduling, and study visit preparation
  • Collect, document, and maintain participant and study-level information in compliance with protocols and SOPs
  • Support specimen handling, inventory management, and investigational product accountability
  • Enter and review research data for accuracy, completeness, and quality assurance
  • Assist with informed consent documentation and participant communication
  • Participate in study team meetings, monitoring visits, and audit preparation activities
  • Learn and apply Good Clinical Practice (GCP), research ethics, and participant safety standards
  • Collaborate with mentors and research professionals to develop clinical research competencies
  • Attend departmental training sessions and professional development opportunities
  • Perform study-related administrative and operational tasks
  • Some roles may involve specimen handling and management of research supplies

Benefits

  • medical and dental care programs
  • generous retirement benefits
  • a wide array of family-friendly and cultural programs
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