Secretario/A Ejecutivo/A Bilingüe (Inglés C1)

General de Galerías Comerciales SOCIMI

Marbella

On-site

EUR 70,000 - 90,000

Full time

14 days+

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Job summary

General de Galerías Comerciales SOCIMI is seeking a Programmer with SAS and R expertise to support German AMNOG dossiers and market access activities from Spain, with remote/hybrid flexibility. The role emphasizes statistical programming, trial data analysis, and cross-functional collaboration with EU-HTA teams.

The ideal candidate holds a Master’s degree or PhD in biostatistics or data science, has >2 years in SAS/R programming, and is fluent in German and English.

Qualifications

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

Responsibilities

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

Skills

SAS programming
R programming
CDISC SDTM/ADaM
Statistical analysis
Automation
Clinical data analysis

Education

Master's degree or PhD in biostatistics, data science, or related field

Tools

SAS
R

Job description

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

Madrid, Spain

Full time

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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