You will need to login before you can apply for a job.Sector: TechnologyRole: Senior ExecutiveContract Type: PermanentHours: Full TimeICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.As a Principal Statistical Programmer, you will be dedicated to one of our global pharmaceutical clients.ResponsibilitiesYou will be responsible for completion of the following:Creating, validating, executing and generating statistical programs consisting of listings, safety and efficacy outputs (analysis datasets, tables, figures)Creating and finalising project or departmental level macrosCreating and finalising programming specifications/mock-upsGenerating accurate, complete and consistent outputs in accordance with documented procedures and project specific timelinesYou will be responsible for leading programming deliverables for at least one study of moderate complexity and/or scope including effective resource planning and tracking and work allocation to ensure project, timeline and quality goals are consistently achieved.Additionally, you will contribute to the review and quality control of programming deliverables, including statistical programs and supporting specifications and documentation. You will effectively liaise with other functions in the conduct of programming activities and support other project activities such as addressing audit findings and facilitating flow of study budget information, as required.QualificationsA strong communicator with a proactive nature and a willingness to work as part of a teamA minimum of 6 years relevant experience of successfully performing the role of Statistical Programmer, preferably in the clinical research industryGood understanding of global clinical trial practices, procedures, methodologies and regulatory requirements (e.g., GCP, ICH)Good working knowledge of the types of risks associated with a study and the impact on key parameters, such as study timelinesStrong working knowledge of statistics and statistical software packagesStrong SAS programming skillsGood working knowledge of statistical conceptsStrong working knowledge of data structures (e.g., CDISC SDTM, ADaM), software development lifecycle and their implementationStrong working knowledge of the development and use of standard programs and macrosAbility to critically review data and implement corrective action steps effectivelyCompanyLearn more about this companyVisit this company’s hub to learn about their values, culture, and latest jobs.
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