Health Technology Assessment Consultant, German

Jobtailor; Barcelona; Presencial; EUR 52.000 - 75.000; Jornada completa

Descripción de la vacante

Jobtailor in Barcelona, Spain is seeking a skilled HTA/AMNOG professional to contribute to German dossiers (Modules 2–4) and to perform scientific assessments of clinical trial data. You will conduct literature reviews, write AMNOG texts, and prepare statements for G‑BA hearings.

The role requires strong data analysis, statistical skills, and fluency in German and English. Collaboration across Market Access, HEOR, and Medical Affairs is essential.

Formación

• 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.

Responsabilidades

• 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.

Conocimientos

HTA

AMNOG

HEOR

Market Access

Medical writing

Statistical analysis

Data analysis

German language

English language

Clinical trial designs

Educación

Master's degree or PhD in life sciences / biostatistics / epidemiology / pharmacy

Herramientas

SAS

R

Python

CDISC SDTM/ADaM

MS Office

Reference management tools

Descripción del empleo

Responsibilities

• 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

• 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

• Affinity for data and excellent analytical and conceptual skills.
• Experience in data analysis (advanced Excel skills); familiarity with Python or 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. Proficient in translating complex data into clear, structured documents while ensuring scientific quality and compliance with HTA standards.