Associate Clinical Programmer

Stellen Nordrhein Westfalen

Clinical data monitoring
Quantitative analytical support
Clinical program support
Participate in the lifecycle of producing key data and/or reports in support of data review reporting development

Job Summary

  • Participate in the lifecycle of producing key data and/or reports in support of data review reporting development.
  • These tasks are to be performed team based with general direction and supervision.
  • Program reports of low to medium complexity from documented requirements, within the clinical reporting systems using SQL, PL/SQL, C#, VB script, SAS, Python, R.

Matching Summary

Participate in the lifecycle of producing key data and/or reports in support of data review reporting development.

Skills & Requirements

Must-have

  • clinical data monitoring
  • quantitative analytical support
  • clinical program support
  • analytics report delivery
  • clinical reporting systems
  • SQL, PL/SQL, C#, VB script, SAS, Python, R

Nice-to-have

  • team-based work
  • general direction and supervision

Key Requirements

  • Clinical Trials
  • Computer Programming
  • Data Analysis
  • Programming Languages

Work Rights

Not specified

Tailored Resume

Cover Letter