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Madrid, Community of Madrid, España
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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
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
Strong 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
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
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
Strong 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