Energy Project Document Controller | Hybrid Role

Vèringer Engineering; Madrid; Hybrid; EUR 50,000 - 75,000; Full time

Job summary

Madrid, Spain-based HTA Programmer role focusing on German AMNOG dossiers and statistical programming in SAS and R. The candidate will analyze clinical trial data, support HEOR and market access activities, and contribute to report automation.

You should have a master's or PhD in biostatistics or data science, with experience in HTA/AMNOG, CDISC SDTM/ADaM, and fluency in German and English. Remote/hybrid work with cross-functional collaboration is offered.

Qualifications

• Master's degree or PhD in biostatistics, data science, or related field.
• Experience in HTA, AMNOG, HEOR or Market Access preferred.
• Familiarity with CDISC SDTM/ADaM standards.
• German AMNOG process knowledge is a plus.

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

Skills

Analytical skills

Data interpretation

Data storytelling

Statistics & data science

SAS programming

R programming

CDISC SDTM/ADaM

Education

Master's degree in biostatistics

PhD in biostatistics or data science

Tools

SAS

R

CDISC SDTM/ADaM

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

Please submit your CV in English.