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    Sr. Statistical Programmer - London, United Kingdom - Lifelancer

    Lifelancer
    Lifelancer London, United Kingdom

    6 days ago

    Default job background
    Full time
    Description

    We are currently looking for an enthusiastic and talented Senior Statistical Programmer willing to be involved in all spectrum of Statistical Programming activities, including acting as Lead Programmer on studies. This role can be home-based in the UK or EU where we have the ability to hire.
    Your core responsibilities:

    • Creation and QC of study specifications for SDTM datasets, and statistical programming and QC of SDTM datasets for Phase I-IV trials.
    • Creation and QC of study specifications for ADaM datasets, and statistical programming and QC of ADaM datasets for Phase I-IV trials.
    • Statistical programming and QC of tables, listings and figures for Phase I-IV trials.
    • Responsible for the quality and timeliness of assigned statistical deliverables.
    • As Lead Statistical Programmer, primarily responsible for all statistical programming activities on assigned studies including planning and coordination of activities for assigned statistical programming team members.
    • Active participation in improvements to departmental processes and procedures.
    • Provide mentoring within the Statistical Programming team.

    This position is perfect for you if you have:

    • BSc/BA or equivalent in computer science, mathematics, statistics, life sciences or related field(s).
    • Excellent SAS programming skills (BASE, MACRO, GRAPH).
    • Excellent knowledge of CDISC standards.
    • Statistical Programming experience within a CRO Pharmaceutical/Healthcare/Biotechnology industries.
    • Experience in statistical programming initiatives, and development of processes.
    • Knowledge and experience in database design and structures.
    • The ability to perform all duties as a statistical programming project team member with no supervision. The ability to perform all duties of Lead Statistical Programmer on several concurrent studies with minimal supervision.
    • Expert knowledge of clinical trial practices, procedures and methodologies.
    • Strong oral and written communication skills.
    • Excellent organizational/time management skills.
    • An excellent investigative and meticulous approach to all activities and tasks.

    Please use the below link for job application and quicker response.

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