Clinical Data Analyst II - European Union - Veeda Lifesciences

    Veeda Lifesciences
    Veeda Lifesciences European Union

    1 hari yang lalu

    Teknik / Arsitektur
    Deskripsi

    Veeda Lifesciences is seeking a Clinical Data Analyst II based in Europe for its growing international hematology/oncology Clinical Trials program.

    This is a full-time job.

    Job overview:

    The Clinical Data Analyst II is responsible for designing, developing, and implementing data-driven analytical solutions that support clinical trial oversight, data quality, and operational excellence. R/SAS is used for data processing, analysis, visualizations, and automated reporting across multiple clinical studies. The analyst collaborates closely with cross-functional teams within the company, including Data Management, Clinical Science and Clinical Operations, to ensure that analyses and insights are fully aligned with the study protocol, meet customer requirements, and support study objectives and operational needs

    Main responsibilities:

    • Design, develop, and automate data analytics and reporting solutions using R, Python, and related tools to deliver meaningful clinical insights.
    • Create standardized reports, dashboards, visualizations, and presentation templates to ensure consistent communication across stakeholders.
    • Produce scheduled and ad hoc clinical study reports (e.g., study status, site performance, safety, visits, drug forecasting) aligned with client and internal requirements.
    • Perform trend analysis and predictive analytics to monitor study performance, quality metrics, and site efficiency, supporting informed decision-making.
    • Collaborate with cross-functional teams to gather reporting requirements and translate them into clear programming and output specifications.
    • Act as a liaison between data teams and business functions to support development of new analytical tools and reports.
    • Manage analytics projects by tracking progress, maintaining documentation, and communicating key findings and milestones.
    • Monitor, document, and coordinate resolution of reporting tool issues to ensure data accuracy and reliability.
    • Maintain compliance with SOPs, programming standards, data protection regulations, and quality and information security management systems.
    • Contribute to continuous improvement of processes, documentation, and reporting standards within clinical operations.

    Job Requirements:

    • Bachelors in Statistics, Biostatistics, Mathematics or another relevant field
    • 2 to 4 years of experience in R/SAS and previous experience with EDC platforms for clinical trials in a CRO, a pharmaceutical or equivalent organization and hands-on experience on analytics tools such as R/RStudio, Python etc.
    • Excellent command of English, both oral and written
    • Proficiency in R programming with experience in data analysis, automation, and reporting
    • Working knowledge of Python or SAS for analytical and reporting solutions
    • Strong capability in developing automated tools, standardized reports, and documentation
    • Ability to analyze, interpret, and present complex data clearly and accurately
    • Strong communicator and collaborative team player with a quality-focused, detail-oriented approach
    • Analytical problem-solver with the ability to manage multiple priorities effectively and meet deadlines

    Join us to be part of a multidisciplinary team of highly skilled scientists and healthcare professionals in the forefront of Clinical Research within a friendly work environment.


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