Statistical Programmer

K-Recruiting Life Sciences; Düsseldorf; Remote; EUR 50.000 - 70.000; Teilzeit

Zusammenfassung

A leading life sciences recruiting firm is looking for a Statistical Programmer. The role involves developing TFLs for HTA / HEOR submissions and conducting analyses. Candidates should hold a relevant degree, possess at least 4 years of experience, and have strong skills in SAS programming. This is a fully remote position with a start date of November 17, 2025, for a duration of 5 months.

Qualifikationen

• B.Sc. in a relevant field required; M.Sc. preferred.
• 4+ years of experience in clinical research.
• Experience in oncology is an advantage.

Aufgaben

• Develop independent TFLs for HTA / HEOR.
• Generate analyses for HTA / HEOR submission and publication.
• Improve programming efficiency with ad-hoc solutions.

Kenntnisse

SAS programming

Statistical analysis

Good understanding of GCP

Advanced English

Ausbildung

Bachelor’s degree in statistics, biostatistics, mathematics, computer science or life sciences

Master’s degree in bio/statistics

Tools

SAS Enterprise Guide

SAS Studio

R

Jobbeschreibung

Statistical Programmer (M / F / D)

Responsibilities

• 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.

Qualifications

• 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

Requirements

• Start: 17.11.2025
• Duration: 5 months
• Capacity: 5 days per week
• Location: 100% remote