Senior Associate, Regulatory Affairs

Role: Senior Associate, Regulatory Operations supporting regulatory activities for Corcept's biopharma portfolio, including hypercortisolism and oncology treatments. Responsibilities: compile, format, publish electronic regulatory submissions; maintain Veeva Vault RIM system and GxP change controls; QC regulatory documents; collaborate with vendors for e-submission files; manage regulatory submission tracker; develop SOPs and support filings. Requirements: BA/BS in scientific discipline; 3+ years in pharmaceutical regulatory functions; experience with Veeva Vault preferred; proficient in Microsoft Office; detail-oriented with strong communication skills; able to manage multiple projects in a dynamic environment. HighValue: regulatory submissions, Veeva Vault, electronic submissions, GxP change control, QC processes. WorkSetup: headquarters-based in the U.S., full-time, with an expected salary range of $125,600-$177,300.