LogoFresh Jobs Ahead
ICON plc
ICON plc
KonsaltingLogistikaSog‘liqni saqlash
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.
LinkedIn
Kompaniyadagi ish o‘rinlari

Remote Clinical Research Associate in Canada

Monitor clinical trials for ICON’s sponsor-dedicated research programs across Canadian sites. Support protocol adherence, reliable data, and patient safety throughout each study.

CAKanadaMasofaviyTo‘liq stavkaJuniorO‘rta darajaTalab Qilinadigan Til: inglizchaKlinik tadqiqot
Google Cloud Platform

Tavsif

  • Manage site qualification, initiation, monitoring, and close-out visits for clinical trials
  • Maintain protocol adherence, data quality, and patient safety throughout the study lifecycle
  • Work with investigators and site teams to support effective study execution
  • Review clinical data and resolve queries to uphold data quality
  • Help prepare and review study materials, including protocols and clinical study reports
  • Design and analyse clinical trials, interpret complex medical information, and support the development of new treatments and therapies
  • Own clinical trial monitoring deliverables while working collaboratively within a sponsor-dedicated model

Talablar

  • Bachelor’s degree in a scientific or healthcare-related discipline
  • At least two years of experience working as a Clinical Research Associate
  • Detailed understanding of clinical trial operations, applicable regulations, and ICH-GCP guidelines
  • Well-organized, detail-oriented communicator with strong coordination skills
  • Able to work independently and collaboratively in a fast-paced setting
  • Available to travel as needed, approximately 60% of the time
  • Legally authorized to work in Canada

Imtiyozlar

  • Base salary with performance-related incentives
  • Health and wellbeing programs, including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programs and wellbeing resources
  • Structured training and career development opportunities

O‘xshash ish o‘rinlari