Administrativo/A Compras Con Inglés (Temporal)

Droguería Venezuela

Telde

Hybrid

EUR 60,000 - 90,000

Full time

14 days+

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Job summary

Droguería Venezuela seeks an experienced HTA programmer to support German health technology assessments with SAS and R analyses. This hybrid Spain-based role involves coding analyses for AMNOG dossiers, meta-analyses, and data-driven insights for market access.

Ideal candidates hold a Master’s in biostatistics or data science, with >2 years in SAS and CDISC SDTM/ADaM, and fluent German and English. Remote/hybrid work in Spain is offered with cross-functional collaboration.

Qualifications

  • Advanced SAS programming and data analysis skills for HTA dossiers.
  • Experience with German AMNOG/HEOR processes is a plus.
  • Familiarity with CDISC SDTM/ADaM datasets and clinical study designs.

Responsibilities

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

Skills

SAS programming
R programming
CDISC SDTM/ADaM
German fluency
English fluency
HTA/HEOR/AMNOG
Statistical analysis

Education

Master's in biostatistics/data science
PhD in biostatistics/data science

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
  • **Solid understanding of core statistical methods** used in clinical trials and HEOR

Personal Competencies

  • Structured, reliable, and quality-driven working style
  • Strong teamwork and communication skills
  • Fluent German and English , written and spoken (this is an absolute must)
  • Strong strategic and critical thinking skills focus on quality, service, and solutions.
  • Well-organized, highly independent, highly motivated
  • Strong customer orientation, a high level of responsibility and reliability
  • High attention to detail, and audit-ready mindset

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