ClinChoice-posted 4 months ago
Full-time • Senior
51-100 employees

ClinChoice is searching for a Senior Statistical Programmer to support our inhouse project. This role offers the opportunity to work directly for a single sponsor while benefiting from the security and additional career opportunities that come with being part of a global CRO. As a client-facing role, we are looking for confident candidates who can work independently while establishing a high-trust environment with the client’s counterparts.

  • Participate in CRF design, database review, data management plan, 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/or 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
  • Responsible for the execution of ad-hoc requests, manuscripts, posters, and presentations
  • Minimum of 10 years of SAS programming in the pharmaceutical or biotechnology industry with a BA/BS in computer science, statistics, math, or MA/MS with 8 years of experience
  • Expertise in SAS programming language, report generation, and standards for programming and validation
  • Experience in the therapeutic area of Rare Disease
  • Experience with CDISC data standards required
  • Experience as a senior statistical programmer at a pharmaceutical 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 required for working successfully in a cross-functional team environment
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