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Statistical Programmer
Zusammenfassung
A leading life sciences recruiting firm is seeking a Statistical Programmer in Dortmund, Germany. You will develop independent TFLs for HTA/HEOR and generate analyses for submission and exploratory purposes. The ideal candidate has a Bachelor's in a relevant field and 4+ years of experience in clinical research. Knowledge of SAS is essential, and R knowledge is recommended. This role is 100% remote, starting on November 17, 2025 for 5 months.
Qualifikationen
- Bachelor’s degree in statistics, biostatistics, mathematics, computer science or life sciences required; 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.
- Excellent English language skills.
- 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.
- Previous experience in SAS macro and/or system utility development is preferred.
- R knowledge is highly recommended.
Aufgaben
- Develop independent TFLs for HTA/HEOR.
- Independently generate analyses for HTA/HEOR submission, publication, exploratory analysis.
- Improve programming efficiency by developing ad-hoc solutions (macros) to speed up TFL creation and validation.
- 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.
- Bachelor’s degree in statistics, biostatistics, mathematics, computer science or life sciences required; 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
- Excellent English language skills
- 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 in SAS macro and / or system utility development is preferred
- R knowledge is highly recommended
- Start: 17.11.2025
- Duration: 5 months
- Capacity: 5 days per week
- Location: 100% remote
* Der Gehaltsbenchmark wird auf Basis der Zielgehälter bei führenden Unternehmen in der jeweiligen Branche ermittelt und dient Premium-Nutzer:innen als Richtlinie zur Bewertung offener Positionen und als Orientierungshilfe bei Gehaltsverhandlungen. Der Gehaltsbenchmark wird nicht direkt vom Unternehmen angegeben. Er kann deutlich über bzw. unter diesem Wert liegen.
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