Health Technology Assessment Consultant, German

IQVIA

HTA Analyst supporting health technology assessment and market access activities in Germany. Contributing to German AMNOG dossier development and collaborating with cross-functional teams.

Posted 7/13/2026full-timeBarcelona • 🇪🇸 SpainJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in developing German AMNOG dossiers and conducting scientific assessments of clinical trial data, with strong capabilities in medical writing and statistical analysis. Proficient in translating complex data into clear, structured documents while ensuring scientific quality and compliance with HTA standards.

Highest-signal resume keywords

German AMNOG Dossier DevelopmentClinical Trial Data AssessmentMedical WritingStatistical AnalysisFluent German and English

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Study DesignStatistical PrinciplesData AnalysisSAS ProgrammingR ProgrammingCDISC SDTM/ADaMSystematic Literature ReviewEvidence SynthesisHTA MethodologyMarket Access

Soft Skills

Analytical SkillsAttention to DetailCommunication Skills

Tools & Technologies

MS OfficeReference Management ToolsPython

Industry Keywords

HTAAMNOGHEORG-BA ProceduresIQWiG

Tech Stack

Tools & technologies

Python

About the role

Key responsibilities & impact

Contribute to the development of German AMNOG dossiers, with a focus on Modules 2–4
Perform scientific assessment of clinical trial data, including efficacy, safety, patient-relevant endpoints, and subgroup analyses
Conduct systematic literature reviews and structured evidence syntheses
Medical writing, including: AMNOG dossier texts and updates
Written statements and responses for G BA procedures and hearings
Scientific reports, slide decks, and selected publications
Support indirect treatment comparisons and interpretation of statistical outputs
Collaborate closely with cross functional teams (Market Access, HEOR, Medical Affairs, EU-HTA Team)
Ensure scientific quality, clarity, and consistency of HTA-related documents
Monitor and interpret methodological developments from IQWiG, G BA, and relevant HTA bodies

Requirements

What you’ll need

Master’s degree or PhD in life sciences, biostatistics, epidemiology, pharmacy, or a related field
Initial experience in HTA, AMNOG, HEOR, or Market Access (industry, consultancy, or research institute preferred)
Solid understanding of clinical study designs, endpoints, and statistical principles
Familiarity with the German AMNOG process, IQWiG methodology, or G‑BA procedures is an advantage
Experience in scientific and medical writing
Strong analytical skills and attention to detail
Ability to translate complex data into clear, structured, and persuasive text
Any of the following skills will be a plus
Affinity for data and excellent analytical and conceptual skills.
Experience in data analysis (advanced excel skills); familiarity with Python or a programming language
Strong background in statistics/data sciences/programming
Proficient in MS Office; experience with reference management tools
>2 years experience in advanced SAS and R programming
>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
Fluent German and English, written and spoken (it’s an absolute must)

Benefits

Comp & perks

Please submit your CV in English