Programmer, SAS, R, German

🕒 September 15

🇪🇸 Spain – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🖥 Software Engineer

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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IQVIA

WebsiteLinkedInAll Job Openings

10,000+ employees

💼 Consulting

🏭 Manufacturing

📣 Marketing

💰 $1G Post-IPO Debt on 2023-05

Consulting • Manufacturing • Marketing

IQVIA is a global leader in data analytics and technology solutions, dedicated to improving health outcomes. The company utilizes its Connected Intelligence platform to harness the power of advanced data analytics and artificial intelligence, facilitating innovation in healthcare. IQVIA focuses on various areas, including clinical research, technology, and consulting services to solve complex healthcare challenges and accelerate the delivery of new therapies to patients.

📋 Description

• 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

• 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

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