Principal Programmer

cslbehring.cz

Design data structure and specifications
Lead production and validation efforts
Ensure quality and accuracy of clinical data
Collaborates with the study teams to design data structure and specifications for ad hoc and study deliverables including, but not limited to ADaM datasets, Tables, Figures, Listings and Analysis Submission content

Job Summary

  • Collaborates with the study teams to design data structure and specifications for ad hoc and study deliverables including, but not limited to ADaM datasets, Tables, Figures, Listings and Analysis Submission content.
  • Leads and oversees the design and implementation of complex SAS programs for applications designed to analyze and report complex clinical trial data in CDISC ADaM format.
  • Works closely with clinical study teams to execute activities to ensure project timelines are met with high quality deliverables.

Matching Summary

Collaborates with the study teams to design data structure and specifications for ad hoc and study deliverables including, but not limited to ADaM datasets, Tables, Figures, Listings and Analysis Submission content.

Skills & Requirements

Must-have

  • design data structure and specifications
  • lead production and validation efforts
  • ensure quality and accuracy of clinical data
  • design and implement complex SAS programs
  • develop global tools for efficiency
  • work closely with clinical study teams

Nice-to-have

  • presentations at professional conferences
  • solutions-oriented mindset
  • networking skills and knowledge sharing

Key Requirements

  • BSc in Computer Science, Mathematics, Statistics or related area
  • At least 8 years of experience in clinical/statistical programming
  • Indepth understanding of CDISC standards (CDASH, SDTM, ADaM)
  • Extensive experience with SAS software and SAS Macros
  • Proven experience in leading programming activities for pooled and exploratory analyses

Work Rights

Not specified

Tailored Resume

Cover Letter