Description
We are looking for a highly motivated HTA Analyst / Consultant to support health technology assessment (AMNOG) and market access activities in Germany. The role is based in Spain, Portugal, or Greece.
Key Responsibilities:
- Contribute to the development of German AMNOG dossiers, focusing on Modules 2–4
- Perform scientific assessments 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 scientific reports
- Support indirect treatment comparisons and interpretation of statistical outputs
- Collaborate with cross-functional teams, including Market Access, HEOR, Medical Affairs, and 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
Your Profile:
- Master's degree or PhD in life sciences, biostatistics, epidemiology, pharmacy, or a related field
- Initial experience in HTA, AMNOG, HEOR, or Market Access
- 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
Benefits: No specific benefits mentioned.
Requirements:
- Fluent German and English, written and spoken
- Structured, reliable, and quality-driven working style
- Strong teamwork and communication skills
- Well-organized, highly independent, and highly motivated