Clinical Research Coordinator

Overview We are seeking a dedicated and detail-oriented Clinical Research Coordinator to join our dynamic research team. In this vital role, you will participate in the operations of clinical trials, ensuring compliance with regulatory standards and maintaining high-quality data collection. Your approach will facilitate smooth study progress, support patient safety, and uphold the integrity of clinical research activities. This position offers an exciting opportunity to contribute to groundbreaking medical advancements while working in a collaborative and innovative environment. Duties Coordinate and manage all aspects of clinical trials, including participant recruitment, scheduling, and follow-up visits. Ensure adherence to FDA regulations, ICH GCP guidelines, and institutional policies throughout the study lifecycle. Review and verify study documentation for accuracy, completeness, and compliance with protocol requirements. Monitor patient progress by collecting vital signs, blood samples through phlebotomy, and tracking adverse events. Conduct data collection and entry, using statistical software to support study outcomes. What we’re looking for Outstanding interpersonal skills Strong written, organizational, and problem‑solving skills Experience in capturing patient medical history and medication Experience with taking vitals Prior experience in a research environment is preferred, or equivalent combination of education and experience in a health-related field is a plus Bachelor’s degree required Join us to be part of a team committed to advancing healthcare through meticulous research practices. Your expertise will directly impact the development of innovative treatments while fostering a culture of excellence in clinical research. Benefits 401(k) Dental insurance Health insurance Paid time off Vision insurance Work Location: In person #J-18808-Ljbffr The Voluntary Protection Programs Participants' Association, Inc