The Drive to Discover. The Experience to Deliver.

Careers At Incyte Corporation

Looking for a challenge and a chance to grow your career?

Then Incyte is the pharmaceutical company for you. While our pipeline demonstrates the ability to compete with much larger pharmaceutical companies in selecting compelling targets and creating high-quality drug candidates, our smaller size enables employees to see the direct impact of their contributions on the direction of the company. Due to our smart, agile culture and cutting-edge science, we delivered a novel, first-to-market product in an unmet medical need in 2011 - the first in the company's history.

Opportunities for taking on new and/or additional responsibilities, in addition to advancement, are a key element in our culture. Add to that a science-based, fast-paced work environment and you’ve got an exciting company in which to work.

In addition to opportunities for growth, we offer an outstanding benefits andcompensation package to help meet personal needs as well.

Take a look at our current openings to find the match that’s right for you!

Incyte Corporation values the talents of our diverse workforce and is proud to be an Equal Opportunity Employer.

SAS Programmer

Department: DMB
Location: Incyte Corporate Headquarters

SAS Programmer   

The SAS Programmer is responsible for applying SEND (the Standard for Exchange of Nonclinical Data) standards and SAS programming to support IND submission.

Essential Functions of the job:

  • Generate nonclinical SDTM datasets according to SEND standard and SAP.
  • Run CDISC validation programs to ensure SDTM datasets are CDISC compliant.
  • Develop standard SAS macros for efficient conversion of nonclinical data to SEND compliant SDTM datasets.
  • Perform data manipulation, analysis and reporting of clinical trial data related to clinical PK utilizing SAS programming.
  • Ensure that all programs, outputs and documentation are consistent with ICH guidelines and are conducted in compliance with company SOPs.
  • Conduct adhoc analyses.
  • Validate programs and associated results produced by other programming colleagues.
  • Work with Clinical Research Organizations, as required, to participate in the oversight and management of programming activities to help ensure quality, timeline and deliverable are met.
  • Work independently with minimum supervision; maintain the overall timeline.
  • Other responsibilities, as necessary.


  • BA/BS degree, preferably in a scientific discipline such as Statistics, Computer Science, Mathematics, etc.
  • 3-5 years of SAS programming experience working with nonclinical or clinical trial data in the Pharmaceutical, Biotech industry or CRO; a MS in statistics or computer sciences is desired.
  • Data Management experience and knowledge of CDISC or SEND standard are highly desirable. 
  • Adept at implementing the latest CDISC or SEND SDTM / ADaM standards.
  • Good SAS programming skills and attention to detail are essential.
  • Highly motivated and able to work well independently.
  • Must be able to work well under timeline pressure.
  • Must be able to work on multiple tasks while coordinating others at the same time.

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