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.

Kompaniyadagi ish o‘rinlari

Clinical Research Associate – Canada Remote

Monitor sponsor-dedicated clinical trials for ICON, a global clinical research organization. Support protocol compliance, reliable data, and patient safety across Canadian trial sites.

1 hafta oldin

Kanada

89 728 $ – 112 160 $ / yil

Masofaviy To‘liq stavka Junior O‘rta daraja Talab Qilinadigan Til: inglizcha Klinik tadqiqot

Google Cloud Platform

Tavsif

Manage site qualification, initiation, monitoring, and close-out visits for clinical trials.
Maintain protocol compliance, data integrity, and patient safety throughout each study.
Partner with investigators and site teams to support efficient study execution.
Review clinical data and resolve queries to uphold data quality.
Help prepare and review study materials, including protocols and clinical study reports.
Support clinical trial design and analysis, interpret complex medical data, and contribute to the development of new treatments.
Own assigned 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 Clinical Research Associate experience.
Detailed understanding of clinical trial operations, applicable regulations, and ICH-GCP guidelines.
Strong organizational and communication abilities with careful attention to detail.
Capacity to work independently and collaboratively in a fast-paced setting.
Availability to travel as needed, approximately 60% of the time.
Legal authorization to work in the country where the position is located.

Imtiyozlar

Competitive base pay with performance-based incentives.
Health and wellness programs, including medical, dental, and vision coverage where applicable.
Retirement and pension plans.
Life insurance and disability coverage.
Employee assistance programs and wellness resources.
Professional development through structured training and career pathways.

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Ochish

Clinical Research Associate – Canada Remote

Monitor sponsor-dedicated clinical trials for ICON, a global clinical research organization. Support protocol compliance, reliable data, and patient safety across Canadian trial sites.

Tavsif

Talablar

Imtiyozlar

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