Overview

About IQVIA

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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

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 or more years experience in advanced SAS programming; R programming skills are an advantage
  • 2 or more 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. xqbhyrx

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