Asistente De Compras Y Producto

Sedatex; Barcelona; Hybrid; EUR 55,000 - 75,000; Full time

Job summary

Sedatex in Madrid, Spain is seeking an HTA Programmer to support German AMNOG dossiers and health technology assessments. The role focuses on statistical programming (SAS & R) and collaboration with cross-functional teams across Market Access, HEOR, Medical Affairs, and EU-HTA.

The candidate should have a strong biostatistics background with experience in clinical data analysis and CDISC SDTM/ADaM, and be comfortable working in a remote/hybrid Spain-based setting while coordinating with German

Qualifications

• Master's or PhD in biostatistics, data science, or related field.
• Initial HTA/AMNOG/HEOR or Market Access experience preferred.
• Solid knowledge of clinical study designs and endpoints.
• CDISC SDTM/ADaM familiarity.

Responsibilities

• Contribute to German AMNOG dossiers with emphasis on statistical analyses for Module 4.
• Analyze clinical trial data for efficacy, safety, and endpoints.
• Perform meta-analyses and indirect treatment comparisons.
• Automate and standardize analysis workflows to improve efficiency and reproducibility.
• Collaborate with Market Access, HEOR, Medical Affairs, and EU-HTA teams.
• Ensure scientific quality and clarity of outputs.

Skills

SAS programming

R programming

CDISC SDTM/ADaM

Biostatistics

Data science

Analytical skills

German language

Education

Master's degree in biostatistics or data science

PhD in biostatistics (preferred)

Tools

SAS

R

Job description

Programmer (SAS & R) with German - Spain-based (remote/hybrid)

Madrid, Spain

Madrid, Spain

Full time

R

We are looking for a highly motivated **HTA Programmer** (Analyst/Consultant) to support health technology assessment (AMNOG) and market access activities in Germany. The role is ideally suited for **biostatisticians** or **data scientists** with a strong interest in applying clinical evidence to reimbursement and market access decision-making. A substantial part of the role involves **statistical programming**.

Key Responsibilities:

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

Your Profile:

Education & Technical Background

• Master's degree or PhD in **biostatistics, data science** , or a related field
• Initial experience in **HTA, AMNOG, HEOR, or Market Access** (industry, consultancy, or research institute preferred) and/or in **clinical development**
• Solid understanding of **clinical study designs, endpoints, and statistical principles**
• Familiarity with **clinical study data** and the corresponding industry standards (CDISC SDTM/ADaM)
• Familiarity with the **German AMNOG process** , IQWiG methodology, or G‑BA procedures is an advantage

Skills

• Strong **analytical skills** and attention to detail
• Ability to translate complex data into **clear and structured output**
• Affinity for data and excellent analytical and conceptual skills
• Strong background in **statistics/data sciences/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