Corcept Therapeutics

Associate Director, Biostatistics

Corcept Therapeutics$183K — $269K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Ph.D. in Statistics, Biostatistics, or Mathematics
  • 5+ years of experience in clinical trial development
  • Proficiency in SAS programming; familiarity with SAS/GRAPH, SAS/MACRO, and R
  • Demonstrated project management skills in clinical development
  • Knowledge of global regulatory guidance for clinical data analyses.

Responsibilities

  • Partner with cross-functional teams on clinical trial design and execution
  • Oversee statistical analysis execution by CROs and independent contractors
  • Collaborate with Statistical Programming for statistical analysis generation
  • Evaluate CDISC data packages for compliance and readiness for submission
  • Stay updated on regulatory requirements and statistical developments
  • Consult internal audit on CRO regulatory compliance regarding statistical SOPs
  • Contribute to development of Corcept Biostatistical SOPs.

Benefits

  • Hybrid work model requiring on-site presence three days a week
  • Engagement in cutting-edge clinical research and development
  • Opportunity to shape standards governance and biostatistical procedures
  • Collaborative work environment with multidisciplinary teams
Full Job Description
The Associate Director of Biostatistics will be responsible for leading the execution of statistical components of Corcept Development programs. This position will manage external statisticians and statistical programmers.

This is a hybrid role typically requiring on-site presence at least 3 days per week.

Responsibilities:
  • Partner with Clinical Development, Regulatory, Manufacturing, and Commercial organizations on the design and execution of clinical trials in the Corcept portfolio
  • Oversee execution of the statistical components of clinical studies by CROs and independent contractors. Manage on-time and quality delivery of CRO-generated analyses results
  • Partner with Statistical Programming in generation of statistical analyses for internal and external presentations, and validation statistical analyses results generated by CROs
  • Partner with Statistical Programming in the evaluation of CDISC electronic data packages for completeness, regulatory standards compliance, and submission readiness
  • Stay current with regulatory requirements for statistical methods of analyses and scientific developments in statistical methods for clinical trials
  • Consult internal audit team in assessing regulatory compliance of CROs with respect to statistical SOPs
  • Participate in standards governance and development of Corcept Biostatistical SOPs

Preferred Skills, Qualifications, and Technical Proficiencies:
  • Knowledge of global regulatory guidance on statistical methods for analyses of clinical data, and global submission requirements
  • Proficiency with statistical programming in SAS. Familiarity with SAS/GRAPH, SAS/MACRO, and R
  • Demonstrated ability to apply complex statistical methods, conduct and interpret the results

Preferred Education and Experience:
  • D. in Statistics, Biostatistics, or Mathematics
  • 5+ years of experience in clinical trial development
  • Demonstrated ability for project management of projects in clinical development
  • Experience managing delivery of statistical projects by CROs

The pay range that the Company reasonably expects to pay for this headquarters-based position is $183,500 - $269,800; 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.

For information on how Corcept collects, uses, discloses, protects, and otherwise processes personal information and an explanation of the rights and choices available to you with respect to your personal information, please refer to our Privacy Notice link.

Corcept appreciates the commitment and hard work of all our team members as we strive to discover and develop novel treatments for patients with serious unmet medical needs.

Please visit our website at: https://www.corcept.com/

Corcept will not conduct interviews via text message or messaging platforms and will not ask you to download anything as part of your interview. Though we use third-party tools to help with advertising our jobs, please be vigilant in checking that the communication is in fact coming from Corcept.

About Corcept Therapeutics

Corcept Therapeutics is a commercial-stage pharmaceutical company engaged in the discovery and development of drugs for the treatment of severe metabolic, oncologic and psychiatric disorders. The company's lead product, Korlym, is a cortisol receptor blocker that modulates the effects of cortisol, a hormone produced by the adrenal gland. Korlym is approved by the U.S. Food and Drug Administration (FDA) for the treatment of patients with Cushing's syndrome who have type 2 diabetes or glucose intolerance. The company is also developing other cortisol modulators, including CORT125134, which is in Phase II clinical trials for the treatment of patients with Cushing's syndrome and solid-tumor cancers. Corcept Therapeutics was founded in 1998 and is headquartered in Menlo Park, California.
Learn more about Corcept Therapeutics
Size
238 employees
Market Cap
$2.1 billion
Industry
Net Income
$106 million
Founded
1998
5 Year Trend
+35.1%
Revenue
$353.8 million
NASDAQ

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