Search the 12 jobs at Corcept Therapeutics

The Associate Director of Biostatistics leads statistical execution in clinical development at Corcept, managing external statisticians and programming teams, ensuring quality statistical analyses, and maintaining compliance with regulatory standards while partnering with various divisions.

The Senior Manager/Manager of Business Analytics at Corcept will lead sales operations, optimize CRM tools, manage analytics projects, and develop data-driven insights to inform senior leadership's strategies. They will oversee the execution of a compensation plan, enhance data flows, and leverage AI tools to drive business improvements.

The Field Reimbursement Manager facilitates communication between sales personnel, specialty pharmacy, and healthcare providers to address access challenges related to the approval and use of Korlym. This role requires expertise in navigating the payor landscape and maintaining relationships to improve access to treatment.

The Digital & Omnichannel Marketing Director will lead strategy development and execution of digital media platforms for Corcept’s endocrinology products. This includes overseeing media engagement, campaign performance metrics, and collaborating with other marketing functions. The role requires a deep understanding of digital promotions, compliance with pharmaceutical regulations, and effective communication of insights to stakeholders.

The Associate Director will lead the strategy and execution of marketing automation and digital content aimed at improving customer experiences for Corcept’s endocrinology products, ensuring effective promotion while adhering to regulatory standards. The role involves collaboration with internal and external teams to optimize marketing tactics and track performance.

The National Account Director will manage relationships with National and Regional Payers and PBMs, developing strategies for market access and reimbursement for Corcept brands. This role involves collaboration with field teams to identify access barriers, delivering economic information to educate payers, and ensuring compliance with US healthcare regulations.

The Safety Science Director is responsible for safety monitoring of Corcept products, leading safety analyses, and developing safety reports. This role involves collaboration with cross-functional teams, mentoring junior scientists, and contributing to regulatory submissions and safety evaluations.

The National Field Training Manager will provide training for newly hired Clinical Specialists and ongoing support for the sales team. Responsibilities include facilitating field rides, developing training frameworks, conducting workshops, and assessing training needs. Travel is required for field training and to ensure effective execution of sales initiatives.

As Sr. Manager, Supply Chain Planning, you will develop comprehensive supply plans to ensure a continuous drug supply for global clinical trials. This role includes scenario planning, providing clinical supply recommendations, overseeing inventory at depots, and collaborating cross-functionally to maintain feasible supply plans.

The Director of Pharmacovigilance Quality Assurance will lead quality operations and compliance activities for drug safety and pharmacovigilance processes. Responsibilities include managing the quality assurance team, ensuring compliance with global regulatory requirements, developing audit plans, supporting inspection readiness, and overseeing training programs and non-compliance investigations.

The Senior Manager of Pharmacokinetics will provide analysis and interpretation of pharmacokinetic and pharmacodynamic data, design human and non-clinical studies, and support regulatory submissions. Key responsibilities include conducting analyses, writing reports, and collaborating across teams to ensure accurate execution of deliverables.

The Quality Operations Manager/Sr. Manager oversees quality assurance for manufacturing activities at Corcept and Contract Manufacturing Organizations. Responsibilities include ensuring compliance with cGMP, managing quality assessments, performing product disposition, and supporting internal and external audit processes. The role requires strong collaboration with cross-functional teams to mitigate compliance risks and drive quality improvements in drug manufacturing.