Clinical Research Coordinator

The OpportunityWe’re looking for a motivated Clinical Research Coordinator to join a growing clinical research team in North Carolina. This is an excellent opportunity for someone who enjoys working directly with patients, supporting clinical trials and contributing to high-quality research in a fast-paced site environment.Key ResponsibilitiesCoordinate clinical research studies from start-up through completion, ensuring activities follow study protocols and regulatory requirements.Recruit, screen and schedule participants for clinical trials.Conduct informed consent discussions and maintain accurate participant documentation.Perform study visits, including patient assessments, vital signs, ECGs and sample collection as required by protocol.Maintain accurate source documentation, case report forms and electronic data capture systems.Monitor participant safety, document adverse events and escalate concerns appropriately.Collaborate with Principal Investigators, research nurses and site staff to ensure efficient study delivery.Maintain compliance with GCP, SOPs and applicable regulatory guidelines.RequirementsPrevious experience as a Clinical Research Coordinator or in a clinical research site environment.Experience supporting patient visits, participant recruitment, screening and study documentation.Knowledge of ICH-GCP, clinical trial protocols and regulatory requirements.Strong organisational skills with the ability to manage multiple studies and competing priorities.Excellent communication and patient-facing skills.Experience with EDC systems and electronic medical records preferred.Phlebotomy, ECG and other clinical assessment experience is advantageous.Why Consider This Opportunity?Join a growing clinical research team.Gain exposure to a variety of clinical trials and therapeutic areas.Work in a collaborative, patient-focused environment.Opportunity to develop your clinical research career.