Administrativo/A Contable H/M

Vinci Construction; Sevilla; Hybrid; EUR 60,000 - 90,000; Full time

Job summary

IQVIA is seeking an HTA Programmer (SAS & R) to support AMNOG dossiers in a Spain-based, remote/hybrid role. The ideal candidate will have a strong biostatistics/data science background and hands-on SAS programming experience in clinical trial analysis, with emphasis on German HTA processes.

You will work with cross-functional teams to analyze trial data, produce robust outputs, and drive automation of analysis workflows while ensuring high-quality, audit-ready deliverables.

Qualifications

• Master's or PhD in biostatistics or data science or related field.
• Initial experience in HTA, AMNOG, HEOR, or Market Access.
• Solid understanding of clinical study designs and endpoints.
• Familiarity with CDISC SDTM/ADaM datasets and industry standards.
• Fluency in German and English is mandatory.

Responsibilities

• Contribute to development of German AMNOG dossiers with focus on programming analyses.
• Analyze clinical trial data for efficacy, safety, endpoints and subgroups.
• Perform meta-analyses and indirect treatment comparisons.
• Automate and standardize analysis workflows for efficiency and reproducibility.
• Collaborate with Market Access, HEOR, Medical Affairs and EUHTA teams.
• Ensure scientific quality and clarity of generated outcomes.
• Monitor IQWiG, G-BA procedures and related HTA guidelines.

Skills

SAS programming

R programming

HTA/AMNOG/HEOR

biostatistics

data science

clinical study design

statistical methods

data analysis

Education

Master's degree or PhD in biostatistics, data science

Tools

SAS

R

CDISC SDTM/ADaM

Job description

Programmer (SAS & R) with German - Spain-based (remote/hybrid)

Madrid, Spain
Madrid, Spain
Full time
R
We are looking for a highly motivated HTA Programmer (Analyst/Consultant) to support health technology assessment (AMNOG) and market access activities in Germany. The role is ideally suited for biostatisticians or data scientists with a strong interest in applying clinical evidence to reimbursement and market access decision-making. A substantial part of the role involves statistical programming.

Key Responsibilities

• Contribute to the development of German AMNOG dossiers, with a focus on programming of statistical analyses for Module 4
• Perform scientific assessment and analysis of clinical trial data, including analysis of efficacy, safety, patient-relevant endpoints, and subgroup analyses
• Perform meta-analyses and indirect treatment comparisons and support interpretation of statistical outputs
• Contribute to the automation and standardization of analysis workflows to ensure efficiency, consistency, and reproducibility
• Collaborate closely with cross functional teams (Market Access, HEOR, Medical Affairs, EU-HTA Team)
• Ensure scientific quality, clarity, and consistency of generated outcomes
• Monitor and interpret methodological developments from IQWiG, G BA, and relevant HTA bodies

Your Profile

Education & Technical Background

• Master's degree or PhD in biostatistics, data science, or a related field
• Initial experience in HTA, AMNOG, HEOR, or Market Access (industry, consultancy, or research institute preferred) and/or in clinical development
• Solid understanding of clinical study designs, endpoints, and statistical principles
• Familiarity with clinical study data and the corresponding industry standards (CDISC SDTM/ADaM)
• Familiarity with the German AMNOG process, IQWiG methodology, or G‑BA procedures is an advantage

Skills

• Strong analytical skills and attention to detail
• Ability to translate complex data into clear and structured output
• Affinity for data and excellent analytical and conceptual skills
• Strong background in statistics/data sciences/programming with a focus on process automation
• >2 years experience in advanced SAS programming , R programming skills are an advantage
• >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 (this is an absolute must)
• Strong strategic and critical thinking skills focus on quality, service, and solutions.
• Well-organized, highly independent, highly motivated
• Strong customer orientation, a high level of responsibility and reliability
• High attention to detail, and audit-ready mindset

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 .

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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