4 дня назад
Programmer (SAS & R) with German – Spain-based (Remote/Hybrid)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Programmer (SAS & R) with German – Spain-based (Remote/Hybrid) (HTA/AMNOG): Developing statistical analyses for German AMNOG dossiers and clinical evidence assessments with an accent on SAS programming, R, meta-analyses, indirect treatment comparisons, and CDISC datasets. Focus on automating reproducible workflows, interpreting efficacy and safety outcomes, and translating complex clinical data into audit-ready outputs.
Location: Madrid, Spain; remote or hybrid
Company
Global provider of clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.
What you will do
- Develop German AMNOG dossiers, focusing on statistical programming for Module 4.
- Assess clinical trial data covering efficacy, safety, patient-relevant endpoints, and subgroup analyses.
- Perform meta-analyses and indirect treatment comparisons and interpret statistical outputs.
- Automate and standardize analysis workflows to improve efficiency, consistency, and reproducibility.
- Collaborate with Market Access, HEOR, Medical Affairs, and EU-HTA teams.
- Monitor methodological developments from IQWiG, G-BA, and other HTA bodies while ensuring scientific quality.
Requirements
- Master’s degree or PhD in biostatistics, data science, or a related field.
- More than 2 years of advanced SAS programming experience; R programming skills are advantageous.
- More than 2 years of hands-on clinical data analysis experience with CDISC SDTM/ADaM datasets.
- Knowledge of clinical study designs, endpoints, statistical principles, and core methods used in clinical trials and HEOR.
- Initial experience in HTA, AMNOG, HEOR, Market Access, or clinical development.
- Fluent German and English, written and spoken, is mandatory; the role is based in Spain.
Culture & Benefits
- Work in a cross-functional environment spanning market access, health economics, medical affairs, and EU health technology assessment.
- Apply clinical evidence to reimbursement and market access decision-making in Germany.
- Work in a structured, quality-driven, and audit-ready environment.
- Contribute to a culture focused on integrity, diversity, inclusion, belonging, and collaboration.
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