In general, the Clinical Research Coordinator I will be responsible for the coordination of patient participation (including screening, recruitment, assessment, and follow-up of study participants), collection and maintenance of study data, ensuring adherence to study activities as described in the protocol, and working with other members of the research team to coordinate all other aspects related to the conduct of the clinical trial or study. Working in the Department/Division of OBGYN Maternal Fetal Medicine Research under the direction of the principal investigator, the Clinical Research Coordinator I will support the coordination of clinical research activities according to clinical research studies or trials managed by the Department/Division.