Neurological Sciences) aimed at improving patient health, disease treatment, and quality of life in individuals who are aging or have neurological, psychiatric, or chronic medical disorders. The work will focus on coordinating, supporting, and administering research participant exams and assessments, engaging with the medical and broader community, and monitoring patient safety and research progress. Coordinate clinical research projects from start to finish to support successful communication, coordination, and work across a multidisciplinary healthcare team and a diverse research team to meet project goals. The Clinical Study Coordinator will be independent, responsible, accountable, self-motivated, a strong and adept communicator, and able to complete detailed tasks accurately and with quality. Adhere to project regulatory protocols (e.g., UNMC, FDA, IRB, HIPAA, lab, sponsor, federal) to meet research participant safety and confidentiality, data quality and security, and successful project operation needs. The Clinical Study Coordinator will be able to work with a diverse team of individuals and maintain effective and professional working relationships in a variety of environments (e.g., clinical, research, community).

Neurological Sciences) aimed at improving patient health, disease treatment, and quality of life in individuals who are aging or have neurological, psychiatric, or chronic medical disorders. The work will focus on coordinating, supporting, and administering research participant exams and assessments, engaging with the medical and broader community, and monitoring patient safety and research progress. Coordinate clinical research projects from start to finish to support successful communication, coordination, and work across a multidisciplinary healthcare team and a diverse research team to meet project goals. The Clinical Study Coordinator will be independent, responsible, accountable, self-motivated, a strong and adept communicator, and able to complete detailed tasks accurately and with quality. Adhere to project regulatory protocols (e.g., UNMC, FDA, IRB, HIPAA, lab, sponsor, federal) to meet research participant safety and confidentiality, data quality and security, and successful project operation needs. The Clinical Study Coordinator will be able to work with a diverse team of individuals and maintain effective and professional working relationships in a variety of environments (e.g., clinical, research, community).