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This position will directly support the diverse clinical research activities  through participation in multiple research projects. The primary purpose of this position is to coordinate and manage clinical trials, providing pediatric clinical researchers the infrastructure and resources to conduct clinical research. The Study Coordinator has direct responsibility for day-to-day activities of several pediatric clinical trials involving both drugs and medical devices. Responsibilities include patient recruitment, study procedures, administration of survey/questionnaires and data collection and maintenance. This Study Coordinator in this position will navigate responsibilities based on protocols currently underway and those in development. Other responsibilities include the initiation and maintenance of IRB and other regulatory procedures.

Opportunities for remote work once on-boarded. 2-3 days per week in the office required after orientation.

The Department  supports research focused on childhood diseases and disorders in the Department and across the University, providing infrastructure for facilitating interdisciplinary and collaborative research efforts, advancing the health of children in NC and beyond.

Research efforts focused on human subjects from pediatric populations are supported by the CRI Pediatric Clinical Research Unit (Peds CRU). CRI Peds CRU provides pediatric clinical researchers infrastructure, including program management, regulatory support, data management, sample processing, training/mentoring, community building, space to conduct visits, and study coordinators.

The CRI serves as a hub, reaching out across the Department of Pediatrics, School of Medicine, the University of North Carolina, and beyond to actively assemble cross-disciplinary researchers. Peds CRU studies include diagnostic tests, early phase therapeutics, cohort studies, and randomized trials, pairing new investigators with experienced ones in the collaboration of these studies. The Department’s organizational component consists of 14 divisions, various off campus sites and additional cost centers, all of which are invited to participate in our clinical trial initiatives.

1 year research/study coordinator experience preferred

The coordinator will demonstrate full knowledge of clinical research principles, methods of data collection and analysis.
The coordinator will demonstrate basic knowledge of statistics and related information technology.
The coordinator must understand all aspects of GCP (Good Clinical Practice) to conduct clinical studies under the regulatory guidelines of the FDA and institutional IRB.
The coordinator must understand protocols and be able teach them to faculty, fellows, and clinic personnel.
The coordinator must possess exceptional interpersonal and communication skills.
The coordinator must have a working knowledge of computers and related research equipment.

1 year research/study coordinator experience preferred

n/a

NC State University is an equal opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, color, national origin, religion, sex, gender identity, age, sexual orientation, genetic information, status as an individual with a disability, or status as a protected veteran.



If you have general questions about the application process, you may contact Human Resources at (919) 515-2135 or workatncstate@ncsu.edu. Individuals with disabilities requiring disability-related accommodations in the application and interview process, please call 919-515-3148.



Final candidates are subject to criminal & sex offender background checks. Some vacancies also require credit or motor vehicle checks. Degree(s) must be obtained prior to start date in order to meet qualifications and receive credit.



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