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Statistical Programmer (M/F/D)
Tasks:
Develop independent TFLs for HTA/ HEOR
Independently generating of analyses to be used primarily for HTA/HEOR submission, publication, exploratory analysis
Independent preparation of analyses in compliance with the standard to be considered
Improve programming efficiency by developing ad-hoc solution (macros) to speed up creation and validation of TFLs
Qualification:
Bachelor’s degree in statistics, biostatistics, mathematics, computer science or life sciences would be ideal; master’s degree in bio/statistics preferred
At least 4 years of experience supporting drug development and/or post marketing in clinical research, Pharmaceutical, CRO or Medical Device setting
Experience in oncology Therapeutic Area and/or in late phase projects is an advantage
Good understanding of GCP and GDPR principles
Advanced working knowledge all SAS language, procedures and options commonly used in clinical trial reporting including the Macro language, BASE SAS, SAS/STAT and SAS/GRAPH. Knowledge of SAS Enterprise Guide and/or SAS Studio is recommended but not required
Previous experience supporting SAS macro and/or system utility development is preferred; R knowledge is highly recommended
Excellent English language skills
Intercultural skills and ability to work remotely with team members in different time zones
Requirements:
Start: 15.03.2026
Duration: 12 months
Capacity: 5 days per week
Location: Remote
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