Associate Director, Statistical Programming

Role: Associate Director, Statistical Programming supporting global rare disease programs within Travere Therapeutics. Main objectives include providing strategic programming input, developing standards, overseeing project execution, and ensuring compliance for clinical trial analyses and submissions. Responsibilities leading programming efforts managing vendors validating datasets preparing regulatory documentation such as SDTM, ADaM, and Define.xml files Qualifications Bachelor's in Statistics, Computer Science, or related field at least 8 years' experience in clinical research with SAS programming including 3-5 years in leadership roles strong knowledge of CDISC standards, regulatory guidelines (ICH, FDA), and submission processes Preferred Master's degree experience with UNIX R vendor management High-Value Supporting phase I-IV trials in rare diseases Delivering clinical datasets and reports for regulatory submissions with an emphasis on accuracy and efficiency. Work setup Hybrid in San Diego, with face-to-face requirements; remote options limited #J-18808-Ljbffr Scorpion Therapeutics