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.The Clinical Research Coordinator will perform all aspects of study execution, from participant recruitment to data management, for assigned studies. The RCMU supports clinical studies for PIs across the UNC research enterprise, offering staff experience in a variety of therapeutic areas and with different trial designs and study populations. There is also significant opportunity for professional development in the areas of study start-up, regulatory support, staff training, and project management.We are seeking a coordinator with a comprehensive scope of research knowledge who has a desire to grow and expand their expertise, abilities, and impact on UNC research. The ideal candidate will work well both independently and as part of a team, possessing both problem-solving initiative and willingness to learn from and collaborate with colleagues. This position requires excellent organizational skills, attention to detail, and an ability to communicate effectively.The candidate should have applied knowledge of GCP and CFR and be able to understand and confidently execute complex protocols. Day to day duties may include, but are not limited to: recruitment and enrollment of study participants, protocol execution, collection and maintenance of data, specimen collection and processing, IRB submissions, REDCap database creation, study tracking and reporting, quality assurance and control, maintenance of GCP and compliance with all regulatory bodies, identification and mitigation of potential issues with processes or protocols, and other duties as assigned.