Job Opportunities API

For more than 25 years, Corcept has been singularly focused on the science of cortisol, a powerful hormone that when unregulated, can play a role in a broad range of diseases. Our commercial portfolio includes treatments for hypercortisolism and oncology, and the company has discovered more than 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today.  Corcept is headquartered in Redwood City, California. To learn more, visit www.corcept.com . The Senior Manager, Commercial Regulatory Operations, will support the end-to-end review and approval process for promotional and non-promotional materials, ensuring timely, compliant, and efficient execution across cross-functional teams. At Corcept, this review process is known as the “Content Review Team” (or “CRT”), which brings together three compliance disciplines (regulatory, legal, and medical) for review and approval of materials. This role will oversee and coordinate CRT logistics and operations with Veeva Vault system management.  This role requires strong organizational skills, familiarity with industry tools, and a collaborative mindset to help drive process excellence, audit readiness, and continuous improvement within a fast-paced, launch-focused environment. This is an excellent opportunity for someone looking to expand their pharmaceutical operations experience while contributing to a patient-centered, mission-driven company aiming to revolutionize the treatment of serious diseases.  This is a hybrid role typically requiring on-site presence at least 3 days per week. Responsibilities:   Manage the end-to-end content review and approval process for promotional and non-promotional materials using the Veeva document management system Drive process improvement and operational efficiency initiatives within the CRT workflow Support system maintenance and enhancements in Veeva PromoMats and MedComms by managing administrative updates and light configuration changes Partner with Marketing teams on the development and maintenance of our claims and reference libraries Collaborate closely with Regulatory, Medical, and Legal colleagues to maintain efficient CRT workflows necessary for review and approval of all product and disease-related content proposed by Marketing, Medical Affairs or other teams and their agencies to communicate with external audiences Lead the planning and facilitation of CRT meetings, managing agenda creation, calendar coordination, expedited review processing, material quality checks, and consensus documentation In partnership with Regulatory colleagues, prepare timely and accurate FDA Form 2253 submissions Monitor and report on approval metrics to drive transparency, accountability, and data‑informed decision‑making across the review process Support prioritization and capacity planning to ensure review activities align with business objectives and key timelines Provide onboarding and training for CRT reviewers and content creators, such as marketers and their agencies, on CRT processes, system navigation, and best practices Provide project oversight and vendor management for ongoing enhancements and upgrades within our Veeva system Preferred Skills, Qualifications and Technical Proficiencies:   Expertise in Veeva PromoMats/MedComms and promotional/non-promotional materi