Director, Statistical Programming

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Corcept is leading the way in the research and development of cortisol modulators, molecules that regulate cortisol activity at the glucocorticoid receptor (GR). To date, we have discovered more than 1,000 selective proprietary cortisol modulators.

In 2012, we received FDA approval of Korlym (mifepristone), the first approved treatment for hypercortisolism (Cushing’s syndrome).

Today, our team and collaborators continue to unlock the possibilities of cortisol modulation as a way to treat serious diseases. With more than 30 ongoing studies across a wide range of disease areas, including endocrinology, oncology, metabolism, and neurology, we remain dedicated to advancing the possibilities of cortisol modulation.

Reporting to the Head of Statistical Programming, the Director, Statistical Programming is responsible for successful execution of study-level, compound-level deliverables and milestones over the drug development life cycle in addition to leading various initiatives for department improvements.

Responsibilities :

• Oversee all programming activities on assigned compounds to ensure high quality and timely deliverables to support Corcept’s growing portfolio.
• Ensure department guidelines are followed and modeled for all deliverables, including the development and validation of statistical programming deliverables.
• Help to grow robust procedures for dataset development and delivery, including developing novel approaches to the validation process (e.g., using R).
• Contribute to establishing operational processes and standards for the statistical programming group, including templates for SDTM, ADaM, and TLFs specifications.
• Transparent communication with department head, peers, and team members of timelines and ability to meet compound or department goals.
• Manage internal and external (CRO) programming resources to ensure on-time and quality delivery of analysis results.
• Evaluate CDISC electronic data packages for completeness and ensure submission readiness of study data packages per CDISC standards and FDA guidance.
• Stay current with regulatory requirements on CDISC and clinical regulatory programming standards, including therapeutic area-specific standards.
• Contribute to initiatives for a new programming environment to host clinical data to enabling future regulatory review and data integration across Corcept-sponsored clinical trials.
• Contribute to the development of SAS macros and tools for repeated program use for exploratory and post-hoc analyses as well as best practices for macro development and validation.
• Manage business relationships with statistical programming vendors for the successful and timely delivery of compound milestones.

Preferred Skills, Qualifications and Technical Proficiencies :

Preferred Education and Experience :

The pay range that the Company reasonably expects to pay for this headquarters-based position is $205,000 - $253,300; the pay ultimately offered may vary based on legitimate considerations, including geographic location, job-related knowledge, skills, experience, and education.

Applicants must be currently authorized to work in the United States on a full-time basis.

Corcept is an Equal Opportunity Employer.

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