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Ballerup

    Clinical Standards Developer Specialist - Ballerup, Danmark - LEO Pharma

    LEO Pharma
    LEO Pharma Ballerup, Danmark

    Fundet i: Talent DK C2 - for 3 dage siden

    Default job background
    Permanent
    Beskrivelse

    Your role




    • Develop and maintain programming solutions, such as standard SAS macros, APIs, tools to support the analysis and reporting of clinical trial data across various trials and clinical development projects
    • Act as a superuser, providing day-to-day support to end-users of our Statistical Computing Environment and our analysis and reporting standards
    • Ensure end-user training and assist with IT-related tasks, such as system upgrades
    • Identify and address the needs of different stakeholders, including data management, statistical programming, biostatistics, and medical writing, providing input for prioritization.
    • Support the technical implementation and adoption of clinical data standards
    • Drive the adoption of clinical data standards from external organizations like CDISC and regulatory authorities
    Your Qualifications


    • Graduate qualification in mathematics, statistics, computer science, life sciences, or a related field, or equivalent work experience
    • Strong proficiency in SAS programming
    • Ability to develop and leverage SAS macros for efficient and scalable programming, automating repetitive tasks, and integrating with other systems
    • Strong knowledge of CDISC standards and regulatory requirements
    • Familiarity with handling and analyzing clinical trial data
    • Excellent attention to detail and accuracy
    • Good communication and interpersonal skills
    • Positive mindset and ability to foster good collegial relations
    • Ability to work both independently and collaboratively in a team environment
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