Clinical Research Coordinator A (CRC A): Primary responsibilities include but are not limited to: 1) Reviewing and comprehending assigned protocols, including study procedures and timelines, to ensure that clinical research and related activities are performed in accordance with protocol, SOP, GCP and applicable regulatory requirement; 2) Facilitating the review of new study agreements and contracts; 3) Assisting with the development of study materials including but not limited to, the informed consent document, case report forms (CRFs), study logs; 4) Recruiting and enrolling study participants, coordinating study visits and serving as liaison between the participant, PI, members of the study team and external Sponsor/CRO teams; 5) Collecting study data, completing source documents, and collecting, processing and shipping biological samples; 6) Completing data entry into electronic databases according to source documents and responding to data clarification requests in a timely manner; 7) Contributing to the maintenance of study files, including but not limited to patient binders, investigator site files and trial master file, as required; 8) Leading or contributing to regulatory submissions and stipulation resolution; 9) Coordinating and attending Investigator Meetings, Site Selection visits, routine monitoring visits, and study close out visits; and 10) Working closely with the study PI and PNTC management team to identify problems, implement approved solutions, and monitor results, as applicable. The Penn Neurogenetics Therapy Center (PNTC) supports a diverse group of neurogenetics investigators and clinical research professionals, involving work on investigator-initiated clinical research studies and complex industry-sponsored, first-in-human trials of gene therapies for neurological diseases.