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Job Description
ClinChoice is seeking a Senior Statistical Programmer Consultant to join one of their clients. ClinChoice is a global full-service CRO with a focus on quality, professional development, and a supportive culture. This client-facing role requires a confident individual capable of working independently and establishing trust with the client's team.Role involves:
  • Participating in CRF design, database review, and data management planning.
  • Producing data listings, summary tables, and graphics for analyses.
  • Integrating data across studies.
  • Testing, documenting, reviewing, and validating programs.
  • Coordinating data transfer and programming standards with CROs and vendors.
  • Validating analysis datasets and TFLs from vendors.
  • Collaborating with Biometrics functions for data analysis activities.
  • Executing ad-hoc requests, manuscripts, posters, and presentations.
Requirements:
  • Minimum of 10 years of SAS programming experience in the pharmaceutical or biotechnology industry with a BA/BS in computer science, statistics, or math, or MA/MS with 8 years of experience.
  • Expertise in SAS programming language, report generation, and programming validation standards.
  • Experience with CDISC data standards.
  • Experience as a senior statistical programmer in a pharmaceutical or CRO within an FDA-regulated environment.
  • Experience with Clinical Study Reports and NDA submissions.
  • Ability to manage multiple tasks and meet deadlines.
  • Excellent verbal, written, and interpersonal skills for cross-functional teamwork.
Role offers:
  • Opportunity to work directly for a single sponsor with the security of a global CRO.
  • Professional development and a supportive culture.
  • Remote work opportunity.
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