Sisnet Developer - Hybrid Insurance Tech Innovator

Atmira; Madrid; Híbrido; EUR 50.000 - 70.000; Jornada completa

Descripción de la vacante

IQVIA in Spain is seeking an HTA Programmer to support German AMNOG dossiers with a focus on statistical analyses and SAS/R programming for Module 4. The role targets biostatisticians or data scientists with a strong interest in reimbursement and market access decisions.

The candidate should have 2+ years in SAS, familiarity with CDISC SDTM/ADaM, and fluent German and English. Hybrid/remote setup in Spain is offered, with cross-functional collaboration across EU teams.

Formación

• Master's degree or PhD in biostatistics, data science, or related field.
• Experience in HTA/AMNOG/HEOR or Market Access (industry, consultancy, or research) preferred.
• Solid understanding of clinical study designs, endpoints, and statistical principles.
• Familiarity with clinical study data and CDISC SDTM/ADaM standards.
• Knowledge of German AMNOG process, IQWiG or G-BA is an advantage.

Responsabilidades

• Develop German AMNOG dossiers with emphasis on SAS/R programming for Module 4 analyses.
• Analyze clinical trial data for efficacy, safety, endpoints, and subgroups.
• Perform meta-analyses and indirect treatment comparisons; support interpretation of results.
• Automate and standardize analysis workflows for efficiency and reproducibility.
• Collaborate with Market Access, HEOR, Medical Affairs, and EU-HTA teams.
• Ensure scientific quality, clarity, and consistency of outputs.
• Monitor methodological developments from IQWiG, IQBa, and HTA bodies.

Conocimientos

SAS programming

R programming

Statistics

Data science

Process automation

CDISC SDTM/ADaM

German language

English language

Educación

Master's or PhD in biostatistics/data science

Herramientas

CDISC SDTM/ADaM

Descripción del empleo

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

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.

• 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

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud.

At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world.

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