Responsibilities
Todos los posibles candidatos deben leer con atención los siguientes detalles de este trabajo antes de presentar una candidatura.

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- Contribute to the development of German AMNOG dossiers, focusing 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.

- Write statements and responses for G‑BA procedures and hearings.

- Develop scientific reports, slide decks, and selected publications.

- Support indirect treatment comparisons and interpret 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

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- 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.

Additional Skills

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- Affinity for data and excellent analytical and conceptual skills.

- Experience in data analysis (advanced Excel skills);
familiarity with Pythonor other programming languages.

- Strong background in statistics/data sciences/programming.

- Proficient in MS Office;
experience with reference management tools.

- More than 2 years of experience in advanced SAS and R programming.

- More than 2 years of 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).

Core Competencies

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

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📌 Health Technology Assessment Consultant, German (Barcelona)
🏢 Jobtailor
📍 Barcelona