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Senior Statistical Programmer (m/w/d) - Fully homebased/remote

TN Germany

Frankfurt

Remote

EUR 60.000 - 100.000

Vollzeit

Vor 21 Tagen

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Zusammenfassung

An established industry player is seeking a Senior Statistical Programmer to join their innovative team. This fully remote position offers the chance to work on cutting-edge projects that advance human health through analytics and technology. The ideal candidate will have extensive experience in SAS programming and statistical analysis, with a strong focus on detail and problem-solving. You'll collaborate with clinical teams to develop high-quality reports and datasets, ensuring compliance with industry standards. If you're passionate about making a difference in the healthcare sector, this role offers great opportunities for career growth and development.

Qualifikationen

  • 5+ years in Statistical Programming within CRO/Pharma.
  • Strong programming experience in SAS and knowledge of statistics.
  • Ability to lead projects and communicate effectively.

Aufgaben

  • Import and validate data for clinical study reports.
  • Develop specifications and write programming code.
  • Create statistical analysis tables and communicate with teams.

Kenntnisse

SAS Programming
Statistical Analysis
Attention to Detail
Problem-Solving
Organizational Skills
Communication Skills
Knowledge of GCP and ICH Guidelines

Ausbildung

Master's in Biostatistics
Bachelor's in Statistics
Bachelor's in Mathematics
Bachelor's in Computer Science

Tools

SAS

Jobbeschreibung

The provided job description is comprehensive and contains relevant information about the role, responsibilities, and requirements. However, its formatting can be improved for better readability and engagement by properly structuring sections with HTML tags such as

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    Senior Statistical Programmer (m/w/d) - Fully homebased/remote, Frankfurt
    Client:

    IQVIA

    Location:

    Frankfurt, Germany

    Job Category:

    Other

    EU work permit required:

    Yes

    Job Reference:

    aaba684b739b

    Job Views:

    2

    Posted:

    28.04.2025

    Expiry Date:

    12.06.2025

    Job Description:

    IQVIA is looking to appoint statistical programmers to utilize the SAS programming language to develop clinical study report materials according to the objectives of a clinical trial for regulatory submissions. Responsibilities include:

    • Import data from various sources
    • Perform quality control checks for data issues
    • Interpret project requirements and develop specifications
    • Write programming code following Good Programming Practices
    • Program SDTM and ADaM datasets
    • Create statistical analysis tables, listings, and figures
    • Validate datasets and outputs
    • Communicate with statisticians and clinical teams
    • Use established standards and SOPs
    • Export data and report materials
    • Provide training and mentoring

    We offer the opportunity to work on innovative projects with cutting-edge technology, in a collaborative environment that fosters career growth and development.

    The Person

    Candidates should possess a Master’s or Bachelor’s degree in Biostatistics, Statistics, Mathematics, or Computer Science, with strong programming experience.

    Key Skills:
    • 5+ years in Statistical Programming within CRO/Pharma with ADaM/SDTM experience
    • Attention to detail, problem-solving, and organizational skills
    • Experience in SAS programming in the healthcare industry
    • Knowledge of statistics and analytical skills
    • Understanding of GCP and ICH guidelines
    • Ability to lead or handle scope and resources independently
    • Effective communication and relationship-building skills

    This role is fully remote and does not qualify for UK visa sponsorship.

    IQVIA is a global leader in analytics, technology, and clinical research services, committed to advancing human health through innovation.

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