Clinical Research Nurse/Clinical Research Coordinator

Clinical Trials Center (CTC) is an independent clinical research site dedicated to conducting high-quality, sponsor-funded clinical trials across a variety of therapeutic areas. We pride ourselves on producing reliable data while providing exceptional care to our study participants. Our team values professionalism, accountability, collaboration, and a commitment to excellence. We are seeking an experienced Clinical Research Nurse / Clinical Research Coordinator to join our growing team. This is a dual-role position that combines nursing responsibilities with hands-on study coordination. The ideal candidate is already experienced in sponsor-funded clinical research and can quickly integrate into an active research environment. Role This position is ideal for a licensed nurse who enjoys both patient care and the operational aspects of clinical research. The candidate will serve as a study coordinator while also utilizing their nursing license to support clinical activities within the research clinic. This is not an entry-level research position. Applicants should have previous experience coordinating sponsor-funded clinical trials and be comfortable independently managing study participants, sponsor expectations, and protocol requirements. Responsibilities Coordinate Phase II-IV sponsor-funded clinical trials from screening through study completion. Conduct study visits in accordance with protocol requirements. Review medical history, concomitant medications, and adverse events with participants. Perform protocol-required clinical procedures within scope of licensure and delegation. Support investigational product preparation and accountability activities as permitted by protocol and site delegation. Assist with participant education and answer protocol-related medical questions within scope of practice. Complete source documentation, eSource, EDC, and query resolution accurately and promptly. Maintain study regulatory documentation and assist with essential document management. Communicate effectively with sponsors, CROs, monitors, laboratories, and study participants. Participate in monitoring visits, audits, and sponsor interactions. Serve as lead coordinator on assigned studies and help ensure enrollment, protocol compliance, and data quality goals are achieved. Collaborate closely with investigators, nurse practitioners, coordinators, regulatory staff, and leadership. Qualifications Required Current Tennessee RN or LPN license in good standing. Minimum of 2 years of sponsor-funded clinical research experience. Previous experience serving as a Clinical Research Coordinator. Strong understanding of ICH-GCP and FDA regulations. Experience with EDC systems and electronic source documentation. Excellent organizational skills and attention to detail. Ability to independently prioritize multiple studies and competing deadlines. Professional communication skills with patients, sponsors, CROs, and monitors. Preferred Experience coordinating pulmonary, respiratory, internal medicine, and metabolic studies. Experience performing clinical assessments, specimen processing, ECGs, spirometry, or other protocol-required procedures. ACRP or SOCRA certification (or willingness to obtain certification). The right candidate is: Able to become productive quickly with minimal onboarding. Comfortable working independently while collaborating closely with the research team. Highly organized and able to manage multiple active studies simultaneously. Adaptable in a fast-paced environment where priorities can shift throughout the day. Committed to providing outstanding participant care while maintaining protocol compliance and data integrity. Proactive, dependable, and willing to take ownership of assigned studies. #J-18808-Ljbffr Clinical Trials Center of Middle Tennessee