ICON plc
ICON plc
ICON plc sog‘liqni saqlash va farmatsevtika sohalariga xizmat ko‘rsatuvchi global shartnoma asosidagi tadqiqot tashkilotidir. Kompaniya faoliyati dastlabki tadqiqotlardan tortib, marketingdan keyingi jarayonlargacha dori vositalarini ishlab chiqishni qo‘llab-quvvatlovchi klinik, konsalting va tijoriy xizmatlarni qamrab oladi. ICON plc markazlashtirilmagan klinik sinovlar, yurak xavfsizligi, dastlabki klinik laboratoriyalar, tibbiy tasvirlash, tartibga solish bo‘yicha ma’lumotlar va real hayot ma’lumotlari kabi yechimlarni taqdim etadi. Shuningdek, kompaniya yurak-qon tomir kasalliklari, onkologiya, ichki kasalliklar, hujayra va gen terapiyalari hamda biosimilyarlar kabi yo‘nalishlarda terapevtik tajribaga ega bo‘lib, klinik dasturlarni rivojlantirishga yordam berish uchun ma’lumotlar tahlilini bemorga yo‘naltirilgan yondashuvlar bilan birlashtiradi.

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.

Tavsif

  • 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

Talablar

  • 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

Imtiyozlar

  • 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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