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    Sr Statistical Programmer - London, United Kingdom - Lifelancer

    Lifelancer
    Lifelancer London, United Kingdom

    1 week ago

    Default job background
    Description

    We are currently looking for an enthusiasticand talented Senior Statistical Programmer willing to be involvedin all spectrum of Statistical Programming activities includingacting as Lead Programmer on studies. This role can be homebased inthe UK or EU where we have the ability tohire.
    Your coreresponsibilities:

    • Creationand QC of study specifications for SDTM datasets and statisticalprogramming and QC of SDTM datasets for Phase IIVtrials.
    • Creation and QC of study specificationsfor ADaM datasets and statistical programming and QC of ADaMdatasets for Phase IIV trials.
    • Statisticalprogramming and QC of tables listings and figures for Phase IIVtrials.
    • Responsible for the quality andtimeliness of assigned statisticaldeliverables.
    • As Lead Statistical Programmerprimarily responsible for all statistical programming activities onassigned studies including planning and coordination of activitiesfor assigned statistical programming teammembers.
    • Active participation in improvementsto departmental processes andprocedures.
    • Provide mentoring within theStatistical Programmingteam.

    Thisposition is perfect for you if youhave:

    • BSc/BA orequivalent in computer science mathematics statistics life sciencesor related field(s).
    • Excellent SAS programmingskills (BASE MACRO GRAPH).
    • Excellent knowledgeof CDISC standards.
    • Statistical Programmingexperience within a CRO Pharmaceutical/Healthcare/Biotechnologyindustries.
    • Experience in statisticalprogramming initiatives and development ofprocesses.
    • Knowledge and experience in databasedesign and structures.
    • The ability to performall duties as a statistical programming project team member with nosupervision. The ability to perform all duties of Lead StatisticalProgrammer on several concurrent studies with minimalsupervision.
    • Expert knowledge of clinical trialpractices procedures and methodologies.
    • Strongoral and written communicationskills.
    • Excellent organizational/timemanagement skills.
    • An excellent investigativeand meticulous approach to all activities andtasks.

    Please use the below link forjob application and quickerresponse.

    RemoteWork :

    No

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