Associate Clinical Research Coordinator

UNC-Chapel Hill•Chapel Hill, NC

10h•Hybrid

About The Position

Position Summary Flexible work arrangements, including virtual/hybrid work locations, are an integral part of the School of Medicine’s Working Forward initiative. As such, this position’s work location is designated as hybrid. Please note that the designated work location is subject to change based on the unit’s business needs. This position will serve as an Associate Clinical Research Coordinator within the Department of Dermatology. The Associate Clinical Research Coordinator is responsible for the execution of clinical research protocols, including leading efforts in gathering, compiling, and reporting data for a variety of research studies. The mission of the UNC -CH Department of Dermatology is fourfold: to conduct clinical, pedagogical, research, and community service activities that benefit the populations of the local University and Triangle communities, state, region, and nation. The Department also functions as an integral unit of the UNC -CH School of Medicine and an active partner in the UNC Health Care System ( HCS ) in its patient care, teaching, research and administration, as these activities concern diseases of the skin. The Department of Dermatology has active clinical and bench research programs to advance the body of knowledge of dermatological care and integration with other specialties. One aspect of this is the Clinical Trials Unit. The UNC Dermatology Clinical Trials Unit is a dynamic and industry-engaged team contributing impactful research and cutting-edge therapies to patients in North Carolina and beyond.

Requirements

Demonstrated pediatric phlebotomy experience in a clinical or healthcare setting is a must for this position.
Ability to perform venipuncture and capillary blood draws on patients across all pediatric age groups, including infants, toddlers, and adolescents, with minimal or no supervision.
Proficiency in using age-appropriate techniques and equipment to ensure patient safety and comfort.
Prior research experience required.
Must be able to use considerable judgement and skills in performing work assignments.
Strong written and verbal communication skills.
Must be able to work and communicate with diverse populations effectively and professionally.
Ability to work independently as well as function as part of a team.
Working knowledge and ability to utilize Microsoft Office Suite tools for data analysis, reporting, and communication.

Nice To Haves

It is highly expected that the candidate has recruited patients for a research study.
Prior clinical research experience preferred.
Knowledge of infection control and specimen handling protocols preferred.
Spanish language skills are preferred.