ICON plc
ICON plc
ICON plc — денсаулық сақтау және фармацевтика салаларына қызмет көрсететін жаһандық келісімшарттық зерттеу ұйымы. Компанияның жұмысы бастапқы зерттеулерден бастап нарыққа шығарудан кейінгі қызметтерге дейін дәрі-дәрмек әзірлеуді қолдайтын клиникалық, консультациялық және коммерциялық қызметтерді қамтиды. ICON plc орталықтандырылмаған клиникалық зерттеулер, жүрек қауіпсіздігі, ерте клиникалық зертханалар, медициналық бейнелеу, реттеуші ақпарат және нақты өмір деректері сияқты шешімдер ұсынады. Сондай-ақ компания жүрек-қантамыр аурулары, онкология, ішкі аурулар, жасушалық және гендік терапиялар, биосимилярлар сияқты бағыттарда терапиялық тәжірибесін қолданып, клиникалық бағдарламалардың ілгерілеуіне көмектесу үшін деректерді талдауды пациентке бағдарланған тәсілдермен ұштастырады.

Statistical Programmer, Clinical Trials — ICON plc (Tokyo Hybrid)

Develop and validate SAS, R, and Python programs supporting clinical-trial data analysis and reporting at ICON plc. Partner with biostatistics and clinical teams on regulatory documentation and treatment-development activities.

Сипаттама

  • Create, validate, and maintain SAS, R, or comparable statistical programs for clinical-trial data processing, analysis, and reporting
  • Work with biostatisticians and clinical teams to clarify project needs and implement statistical analyses accurately
  • Draft and review statistical analysis plans and programming specifications in line with regulatory expectations
  • Maintain data quality and comply with applicable industry standards, including ICH/GCP guidelines, throughout programming activities
  • Contribute to clinical study reports and other materials submitted to regulatory authorities
  • Produce high-quality statistical programming deliverables in collaboration with project stakeholders and colleagues

Талаптар

  • Bachelor’s degree in statistics, computer science, mathematics, or a related field
  • Demonstrated clinical-research experience as a statistical programmer, including a strong understanding of statistical methods
  • Working knowledge of SAS, R, or Python and experience with clinical data management systems
  • Strong analytical and problem-solving abilities, careful attention to detail, and the capacity to work independently or collaboratively
  • Clear communication skills, including the ability to explain complex statistical topics to non-technical stakeholders
  • Legal authorization to work in the country where the position is located

Артықшылықтар

  • Base salary with performance-based incentives
  • Health and wellbeing programs, including medical, dental, and vision coverage where applicable
  • Retirement and pension programs
  • Life assurance and disability coverage
  • Employee assistance programs and wellbeing resources
  • Professional development through structured training and career progression pathways

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