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Principal Statistical Programmer

Cytel Software Corporation Millcreek, Utah
programmer analysis programming data written sas programming sdtm growth senior lead data manipulation team drug development
September 21, 2022
Cytel Software Corporation
Millcreek, Utah
FULL_TIME

Cytel provides unrivaled biostatistics and operations research knowledge to our customers in the life sciences industries in the form of both software and services.  At Cytel, we work hard to create successful careers with significant professional growth for our employees, as a result of which they work hard to make Cytel successful. Cytel is a place where talent, experience and integrity come together to advance the state of clinical development.

 

As a Senior/Principal Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Phase I-IV clinical trials.  You will report to the Director, Statistical Programming.

 

You will contribute by:

  • performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy, utilizing SAS programming;
  • applying your CDISC know-how and proficiency in SDTM and ADaM, to create and validate datasets/analysis files, tables, listings, and figures ( TLF s);
  • generating complex ad-hoc reports
  • preparing and validating submission packages, i.e. define.xml, Reviewers Guide
  • applying your strong understanding/experience with Efficacy analysis;
  • preparing submission packages
  • performing lead duties when called upon;
  • serving as team player, with a willingness to go the extra distance to get results, meet deadlines, etc.;
  • being adaptable and flexible when priorities change

 

What we are looking for:

 

  • Bachelor's degree or equivalent, preferably in a scientific discipline such as Statistics, Computer Science, Mathematics, etc.
  • Minimum 5 years of SAS programming experience in the Pharmaceutical & Biotech industry.
  • Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials' data.
  • Strong SAS data manipulation, analysis and reporting skills.
  • Ability to implement the latest CDISC SDTM / ADaM standards (production/validation).
  • Proficiency in SAS  MACRO development
  • Strong ad-hoc reporting   
  • Solid experience in Efficacy analysis
  • Experience with Pinnacle21
  • Submissions experience utilizing define.xml and other submission documents.
  • Experience supporting Neurological Disorders (i.e. Multiple Sclerosis, HIV, Alzheimer's, Strokes), strongly desirable.
  • Excellent analytical & troubleshooting skills.
  • Ability to provide quality output and deliverables, in adherence with challenging timelines.
  • Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners.

 

What's in it for you:

 

  • You will have the opportunity to play an integral role helping our clients and the industry shape the future of drug development
  • You will be part of an exciting new chapter in Cytel's history with high growth and opportunities to progress in Senior and Leadership positions within the company
  • Work in an environment designed for an entrepreneurial minded person with a lot of energy, ideas and courage for their implementation
  • Work with and leverage the best and brightest minds in the industry

 

 

Cytel Inc. is an Equal Employment / Affirmative Action Employer. Applicants are considered for all positions without regard to race, color, religion, sex, national origin, age, veteran status, disability, sexual orientation, gender identity or expression, or any other characteristics protected by law.

Cytel does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact Cytel's human resources department to obtain prior written authorization before referring any candidates to Cytel. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and Cytel. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of Cytel. Cytel shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies.

 

#LI-KO1

#CYTELINT


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