HTA Analyst for German Market (AMNOG) - based in Portugal, Spain or Greece (home-based or hybrid)

IQVIA Inc; Hamburg; Remote; EUR 60,000 - 90,000; Full time

Job summary

IQVIA is seeking an HTA Analyst/Consultant to be based in Spain, Portugal or Greece and to support health technology assessment (AMNOG) and market access activities in Germany. The role suits scientists or biostatisticians with a strong interest in applying clinical evidence to reimbursement and decision-making.

A substantial part involves medical writing. You will develop AMNOG dossiers, perform literature reviews, and collaborate with cross-functional teams to ensure high-quality, compliant

Qualifications

• Master’s degree or PhD in life sciences, biostatistics, epidemiology, pharmacy, or 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

Responsibilities

• 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

Skills

HTA AMNOG HEOR Market Access

Clinical study designs & statistics

Fluent German & English

Medical writing

Education

Life sciences/biostatistics/epidemiology/pharmacy MSc/PhD

Tools

SAS

R programming

Python

MS Office

Job description

Madrid, Spain

Vienna, Austria

Munich, Bavaria, Germany

Porto Salvo, Portugal

Frankfurt, Hesse, Germany

Berlin, Germany

Hamburg, Hamburg, Germany

Full time

R1571831

Please note that fluency in German language is an absolute must for this role.

Please note that this role is available in Portugal, Spain or Greece. We advertise it also in Germany ad Austria, so that it can reach a bigger audience.

Job Description:

We are looking for a highly motivated HTA Analyst / Consultant to be based in Spain, Portugal or Greece and to support health technology assessment (AMNOG) and market access activities in Germany (no travels required). The role is ideally suited for scientists or biostatisticians with a strong interest in applying clinical evidence to reimbursement and market access decision-making. A substantial part of the role involves medical writing .

Key Responsibilities:

• Contribute to the development of German AMNOG dossiers, with a focus onModules 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

Your Profile:

Education & Technical Background

• 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

Medical Writing & Analytical Skills

• 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

Personal Competencies

• Structured, reliable, and quality-driven working style

• Strong teamwork and communication skills

• Fluent German and English , written and spoken ( it’s an absolute must )

• Strong strategic and critical thinking skills focus on quality, service, and solutions.

• Well-organized, highly independent, highly motivated

• Strong customer orientation, confident presentation skills, and a high level of responsibility, reliability, and good communication skills

• High attention to detail, and audit-ready mindset

Please submit your CV in English.

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com .

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

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