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.

Clinical Research Associate – Canada Remote | ICON plc

Monitor respiratory and cardiovascular clinical trials for ICON Strategic Solutions across Canada's Greater Toronto Area. Coordinate site visits, compliance, data quality, and guidance for clinical research teams.

Tavsif

  • Manage clinical trial activities in line with study protocols, regulations, and industry standards
  • Drive monitoring activities focused on quality and ongoing process improvement
  • Evaluate site compliance with protocols, regulations, and Good Clinical Practice requirements
  • Complete site visits to review performance, address issues, and support effective study delivery
  • Partner with cross-functional teams to ensure accurate, timely data collection and reporting
  • Train and advise site staff and fellow Clinical Research Associates
  • Develop and sustain productive relationships with site teams and other stakeholders
  • Monitor respiratory and cardiovascular studies throughout the Greater Toronto Area

Talablar

  • Bachelor's degree in a relevant scientific or healthcare discipline
  • Extensive Clinical Research Associate experience with a strong grasp of clinical trial operations and regulatory obligations
  • Demonstrated ability to oversee multiple sites and projects concurrently
  • Strong planning, organization, and problem-solving capabilities
  • Advanced knowledge of monitoring methods, data integrity, and site management
  • Proficiency with applicable clinical trial software and tools
  • Highly effective communication, interpersonal, and stakeholder management skills
  • Ability to influence others and promote compliance in a complex setting
  • Availability to travel as needed, approximately 60%
  • Legal authorization to work in the country where the position is based

Imtiyozlar

  • Competitive base pay with performance-based incentives
  • Health and wellness programs, including medical, dental, and vision coverage where available
  • Retirement and pension provisions
  • Life insurance and disability protection
  • Employee assistance programs and wellbeing resources
  • Structured training, professional development, and career progression opportunities

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