Remote (Global)

ClinChoice is hiring a 1105# Principal Statistical Programmer (Permanent role)

About the Role

ClinChoice is hiring a Principal Statistical Programmer to support our in-house projects. Our mission is to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. In this client-facing role, you will work independently while establishing a high-trust environment with client counterparts.

What You'll Do

  • Participate in CRF design, database review, data management plan development, data review, data validation procedures, and review of data listings.
  • Produce data listings, summary tables, and graphics for interim and final analyses.
  • Integrate data across studies within a project.
  • Test, document, review, and validate all programs according to department guidelines.
  • Coordinate data transfer and programming standards with CROs and vendors.
  • Validate analysis datasets and TFLs from vendors.
  • Collaborate with other Biometrics functions for all activities related to the analysis of clinical trial data.
  • Execute ad-hoc requests, and support manuscripts, posters, and presentations.

What We're Looking For

  • A minimum of 10 years of SAS programming in the pharmaceutical or biotechnology industry with a BA/BS in computer science, statistics, or math; or an MA/MS with 8 years of experience.
  • Expertise in the SAS programming language, report generation, and standards for programming and validation.
  • Therapeutic area experience in Oncology.
  • Experience with CDISC data standards is required.
  • Experience as a senior statistical programmer at a pharmaceutical company or CRO working in an FDA-regulated environment.
  • Experience with Clinical Study Reports and NDA submission.
  • Ability to work on multiple tasks simultaneously and meet project deadlines.
  • Excellent verbal, written, and interpersonal skills for working successfully in a cross-functional team environment.

Technical Stack

  • SAS
  • CDISC data standards

Team & Environment

You will collaborate with other Biometrics functions. We believe our employees are our most valuable asset and use close management and training to develop and maintain highly-qualified personnel.

Work Mode

This is a global role based in the United States.

ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity.

Required Skills
SASCDISCSDTMADaMStatistical ProgrammingClinical TrialsRegulatory SubmissionsMacro DevelopmentData ValidationTLFStudy Data
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About company
ClinChoice

A global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies.

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Job Details
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Posted 7 months ago