HTA Analyst for German Market (AMNOG)

Location: Home-based or hybrid, based in Spain, Portugal or Greece; the role supports German market activities and requires no travel.

Company

hirify.global provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

• Contribute to German AMNOG dossiers, especially Modules 2–4.
• Assess clinical trial evidence, including efficacy, safety, patient-relevant endpoints, and subgroup analyses.
• Conduct systematic literature reviews and structured evidence syntheses.
• Write AMNOG dossier texts and updates, G-BA statements and hearing responses, scientific reports, slide decks, and selected publications.
• Support indirect treatment comparisons and interpret statistical outputs.
• Collaborate with Market Access, HEOR, Medical Affairs, and EU-HTA teams while ensuring the quality, clarity, and consistency of HTA documents.

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, preferably in industry, consultancy, or a research institute.
• Solid understanding of clinical study designs, endpoints, and statistical principles.
• Experience in scientific and medical writing, with the ability to translate complex data into clear, structured, and persuasive text.
• Fluent German and English, written and spoken; German is an absolute must.
• Strong analytical, strategic, critical-thinking, teamwork, communication, presentation, and customer-orientation skills.
• Structured, reliable, independent, quality-driven, and highly motivated working style with strong attention to detail and an audit-ready mindset.

Nice to have

• Familiarity with the German AMNOG process, IQWiG methodology, or G-BA procedures.
• Advanced Excel and data-analysis skills; familiarity with Python or another programming language.
• Strong background in statistics, data science, or programming.
• Proficiency in MS Office and experience with reference-management tools.
• More than 2 years of advanced SAS and R programming experience.
• More than 2 years of hands-on clinical data-analysis experience with CDISC SDTM/ADaM datasets.
• Solid understanding of statistical methods used in clinical trials and HEOR.

Culture & Benefits

• Home-based or hybrid work from Spain, Portugal, or Greece.
• No travel is required for the role.
• Cross-functional collaboration across Market Access, HEOR, Medical Affairs, and EU-HTA teams.
• Work in a quality-focused environment supporting healthcare and life-sciences decision-making.

Hiring process

• Submit a truthful and complete CV in English.
• False statements, misrepresentations, or material omissions may result in disqualification or termination.