Programmer, SAS, R, German

IQVIA

. Contribute to the development of German AMNOG dossiers, focusing on statistical analyses for Module 4 .

Posted 9/15/2026full-timeRemote • SpainJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in statistical analysis and clinical data evaluation, with a strong focus on German AMNOG dossiers and HTA processes. Proficient in advanced SAS programming and familiar with CDISC standards, ensuring high-quality outcomes in collaboration with cross-functional teams.

Highest-signal resume keywords

Advanced SAS ProgrammingClinical Data AnalysisGerman AMNOG ProcessStatistical AnalysisFluent German and English

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

BiostatisticsData ScienceStatistical PrinciplesMeta-AnalysisProcess AutomationR ProgrammingClinical Study DesignCDISC SDTM/ADaM StandardsEfficacy and Safety AnalysisSubgroup Analysis

Soft Skills

Strong TeamworkCommunication SkillsStrategic ThinkingCritical ThinkingAttention to Detail

Certifications & Qualifications

Master’s Degree or PhD in Biostatistics or Related Field

Industry Keywords

HTAAMNOGHEORMarket AccessIQWiGG-BAClinical Development

About the role

Key responsibilities & impact

Contribute to the development of German AMNOG dossiers, focusing on statistical analyses for Module 4
Perform scientific assessment and analysis of clinical trial data, including efficacy, safety, patient-relevant endpoints, and subgroup analyses
Perform meta-analyses and indirect treatment comparisons and support interpretation of statistical outputs
Automate and standardize analysis workflows for efficiency, consistency, and reproducibility
Collaborate with Market Access, HEOR, Medical Affairs, and EU-HTA teams
Ensure scientific quality, clarity, and consistency of generated outcomes
Monitor and interpret methodological developments from IQWiG, G-BA, and relevant HTA bodies

Requirements

What you’ll need

Master’s degree or PhD in biostatistics, data science, or a related field
Initial experience in HTA, AMNOG, HEOR, Market Access, or clinical development
Solid understanding of clinical study designs, endpoints, and statistical principles
Familiarity with clinical study data and CDISC SDTM/ADaM standards
Familiarity with German AMNOG process, IQWiG methodology, or G-BA procedures is advantageous
Strong background in statistics, data science, and programming, with a focus on process automation
>2 years experience in advanced SAS programming
R programming skills are an advantage
>2 years hands-on clinical data analysis experience with CDISC SDTM/ADaM datasets
Solid understanding of core statistical methods used in clinical trials and HEOR
Fluent German and English, written and spoken (absolute must)
CV must be submitted in English
Structured, reliable, quality-driven, and highly independent working style
Strong teamwork, communication, strategic thinking, and critical thinking skills
High attention to detail and audit-ready mindset

Benefits

Comp & perks

Diversity, inclusion, and belonging culture
Opportunity to work with talented employees worldwide
Opportunity to contribute to innovative healthcare and improve patient outcomes