Auxiliar Técnico Educativo/A

Hace 21 horas

Murcia, Region of Murcia, España Grupo El Castillo Jornada completa
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 .

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

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. Learn more at .

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