Serve as the Clinical Data Management Lead on one or more studies and performs hands-on clinical data management tasks to support clinical studies, including, but not limited to the following: reviewing protocols, designing eCRFs, performing UAT, documenting edit check specs, QC'ing external data, reviewing eCRF data, running SAS datasets, coding MH, AE, and CM data, and ensuring database lock activities are completed. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, hyperphagia in Prader-Willi syndrome, endometriosis and uterine fibroids , as well as a robust pipeline including multiple compounds in mid- to late-phase clinical development across our core therapeutic areas.