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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.


Senior Manager, Medical Coding

Department: Development Operations
Location: Incyte Corporate Headquarters

Senior Manager, Medical Coding

The Senior Manager, Medical Coding is responsible for overseeing all aspects of coding, the Coding Specialist(s), setting priorities, coordinating work load, ensuring coding accuracy and consistency and meeting all coding timelines/deliverables.  This is an in-office position based in Wilmington, DE.

Job Responsibilities

  • Oversees all aspects of the coding of medical terms (e.g., adverse events, medical history terms, prior and concomitant medications)
  • Maintains the coding dictionaries (MedDRA and WHODD) and knowledge of structure changes so to assess necessary adjustments
  • Manages dictionary upgrades
  • Generates and maintains synonym lists, coding conventions and coding guidelines
  • Provides advice for data analysis of coded terminology and acts as primary contact in regard to dictionary requests and concerns

Minimum Requirements

  • Bachelorís degree in health science.  Commensurate experience will be considered.
  • 7+ years industry experience in pharmacovigilance, clinical research, and/or clinical data management required
  • 8 years coding experience
  • Expertise in medical terminology & coding is essential.
  • Excellent written and oral skills and demonstrated ability to work both independently and within cross functional teams.
  • Experience with MedDRA and WHODD is required
  • Strong attention to detail and a commitment to high quality work
  • Experience in Oncology is preferred

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