Senior/Principal Statistical Programmer/Analyst Consultant (Cardiovascular, Renal)-Remote -Outside IR35

Added
19 hours ago
Type
Contract
Salary
Salary not provided

Related skills

programming sas clinical trials cdisc sdtm

๐Ÿ“‹ Description

  • Delivery-focused SAS programming lead/support for CVRM studies
  • Work under Programming team leader to deliver programming components
  • Client-facing role with independence and high-trust collaboration
  • Develop, validate, and maintain SAS programs for analysis/reporting
  • Collaborate across Biostatistics, Data Management, Clinical teams
  • Support regulatory submissions and study planning as needed

๐ŸŽฏ Requirements

  • Strong SAS programming experience within pharmaceutical/CRO
  • Hands-on CVRM (Cardiovascular, Renal & Metabolism) study support
  • Experience generating/validating SDTM, ADaM, and TLFs
  • Good understanding of CDISC standards and clinical trial processes
  • Ability to manage multiple priorities independently in a fast-paced environment
  • Experience supporting regulatory submissions is preferred

๐ŸŽ Benefits

  • Client-facing CRO environment with stability and growth opportunities
  • Global CRO with strong training and career development
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