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Assistant Clinical Research Coordinator

Job in Raleigh, Wake County, North Carolina, 27601, USA
Listing for: NC State College of Engineering
Full Time, Part Time position
Listed on 2026-10-15
Job specializations:
  • Research/Development
    Clinical Research, Research Assistant/Associate
Salary/Wage Range or Industry Benchmark: 46000 - 47000 USD Yearly USD 46000.00 47000.00 YEAR
Job Description & How to Apply Below
Posting Details

Job Posting Information

Posting Number PG195255SP Internal Recruitment No Working Title Assistant Clinical Research Coordinator Anticipated Hiring Range $46,000-$47,000 Work Schedule Core Business

Hours:

Monday–Friday, 8:00 a.m.–5:00 p.m.; schedule may vary based on departmental needs. Job Location Raleigh, NC Department Lampe Joint Department of BME

About the Department

The Lampe Joint Department of Biomedical Engineering UNC/NCSU stresses the application of science and engineering, mathematical analysis, and computer techniques to biomedical problems. The research and entrepreneurship of the faculty, students, and staff aim to accumulate, generate and disseminate biomedical engineering knowledge to improve health care for the benefit of the people of North Carolina, the nation, and the world.

Wolfpack

Perks and Benefits

As a Pack member, you belong here, and can enjoy exclusive perks designed to enhance your personal and professional well-being. As you consider this opportunity, we encourage you to review our Employee Value Proposition and learn more about what makes NC State the best place to learn and work for everyone.

What We Offer
  • Medical, Dental, and Vision
  • Flexible Spending Account
  • Retirement Programs
  • Disability Plans
  • Life Insurance
  • Accident Plan
  • Paid Time Off and Other Leave Programs
  • 12 Holidays Each Year
  • Tuition and Academic Assistance
  • And so much more!

Attain Work-life balance with our Childcare benefits, Wellness & Recreation Membership, and Wellness Programs that aim to build a thriving wolfpack community.

Disclaimer:
Perks and Benefit eligibility is based on Part-Time or Full-Time Employment status. Eligibility and Employer Sponsored Plans can be found within each of the links offered.

Essential

Job Duties

As the Research Coordinator, you will coordinate research activities involving participants, clinicians, and members of the research team. You will manage scheduling, support participant recruitment and initial screening, coordinate research procedures and supporting tests, and maintain accurate research data and records. Working within established research protocols and under the guidance of senior team members, you will help ensure research activities are organized, accurately documented, and conducted in accordance with approved procedures.

Key Responsibilities
  • Coordinate schedules for research participants, clinicians, researchers, and facilities; arrange research activities through email and phone communication.
  • Recruit potential participants through local clinics, hospitals, and on- and off-campus outreach activities.
  • Conduct initial participant screening and explain established research procedures.
  • Support research procedures and participant testing in accordance with established protocols, ethical requirements, and department policies.

If you are organized, detail-oriented, and enjoy working directly with research participants and multidisciplinary teams, this position offers an opportunity to contribute to research that supports improved understanding and outcomes for patients and communities.

Other Responsibilities

In addition to the core responsibilities of this role, there may be occasional opportunities to take on additional duties. This offers an opportunity to build on your skills, explore new areas, and gain a deeper understanding of the department’s operations.

Qualifications

Minimum Experience/Education

Bachelor’s degree; or an equivalent combination of training and experience.

All degrees must be received from appropriately accredited institutions.

Preferred Qualifications

  • Background supporting human subjects or clinical research activities.
  • Familiarity with participant recruitment, screening, or research data collection.
  • Proficiency using electronic databases to…
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