Programmer with German language - German HTA submissions – Spain-based (remote/hybrid)

IQVIA LLC; España; Hybrid; PHP 3,149,055 - 4,898,530; Full time

Job summary

IQVIA LLC is seeking a highly motivated HTA Analyst-Programmer to support health technology assessment and market access activities in Germany. This role requires expertise in statistical programming and a strong background in biostatistics or data science.

The ideal candidate will have over two years of experience in SAS programming, solid analytical skills, and fluency in both German and English. This position offers flexibility with remote or hybrid working options.

Qualifications

• Initial experience in HTA, AMNOG, HEOR, or Market Access preferred.
• >2 years experience in advanced SAS programming.
• >2 years hands-on clinical data analysis experience with CDISC SDTM/ADaM datasets.

Responsibilities

• Develop German AMNOG dossiers focusing on statistical analyses for Module 4.
• Perform scientific assessment and analysis of clinical trial data.
• Contribute to automation and standardization of analysis workflows.

Skills

Analytical skills

Attention to detail

SAS programming

R programming

Clinical data analysis

Education

Master's degree or PhD in biostatistics or data science

Tools

CDISC SDTM/ADaM

Job description

## Programmer with German language - German HTA submissions – Spain-based (remote/hybrid)Applylocations: Madrid, Spain: Barcelona, Spaintime type: Full timeposted on: Posted Todayjob requisition id: R1542578**About IQVIA:**IQVIA is a fast-growing and highly successful business, delivering data-driven insights and measurable impact for clients across the global life sciences ecosystem. Leveraging access to some of the world’s most comprehensive healthcare data, advanced analytics and research capabilities, IQVIA experts design and deliver innovative, technology-enabled evidence programs to support decision-making across the product lifecycle.**Job Description:**We are looking for a highly motivated **HTA Analyst-Programmer** 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 mindsetPlease submit your CV in English.