The Semel Institute is seeking to hire a full time Clinical Research Coordinator (CRC) who will contribute to the overall operational management of clinical research / trial / study activities from design to closeout. You will be responsible for the implementation of research activities for one or more studies. In this role you will recognize and perform necessary tasks to manage projects and prioritizes work to meet necessary deadlines. You are also responsible for planning and organizing necessary tasks to ensure adherence to the study protocol and applicable regulations, such as institutional policy and procedures, FDA Code of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP). Collaboration with the Principal Investigator (PI), ancillary departments, central research infrastructure teams, sponsors, institutions, and other entities as needed to support the administration of all aspects of studies including, but not limited to, compliant conduct, financial management, and adequate personnel support is also essential to this role. 

Pay Range: $33.63 – $54.11 hourly