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 – Respiratory and Cardiovascular Trials, Canada Remote

Monitor respiratory and cardiovascular clinical trials for ICON’s sponsor-dedicated research operations. Oversee GTA sites, compliance, data quality, and trial delivery.

Tavsif

  • Manage clinical trial activities in line with protocols, regulations, and industry standards
  • Lead monitoring activities with an emphasis on quality and ongoing improvement
  • Verify site compliance with study protocols, regulations, and Good Clinical Practice standards
  • Conduct site visits to evaluate performance, resolve concerns, and provide operational support
  • Coordinate with cross-functional teams to ensure accurate, timely data collection and reporting
  • Train and mentor site personnel and fellow Clinical Research Associates
  • Develop and maintain effective relationships with site teams and key stakeholders
  • Monitor respiratory and cardiovascular studies across the GTA

Talablar

  • Bachelor’s degree in a relevant scientific discipline or healthcare-related field
  • Extensive Clinical Research Associate experience, with a strong grasp of clinical trial procedures and regulatory requirements
  • Demonstrated ability to manage multiple sites and projects concurrently, supported by strong organizational and problem-solving skills
  • Advanced knowledge of monitoring methods, data integrity, and site management
  • Proficiency with relevant clinical trial software and tools
  • Strong communication, interpersonal, and stakeholder management capabilities
  • Ability to influence others and promote compliance in a complex environment
  • Willingness to travel as needed, approximately 60%
  • Legal authorization to work in the country where the role is based

Imtiyozlar

  • Competitive base pay with performance-related 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
  • Structured training, learning, and career development opportunities

O‘xshash ish o‘rinlari

Air Liquide

Finance Trainee – French, German or Dutch Speaker

Air Liquide

Join Air Liquide’s finance trainee program to support accounting, treasury and reconciliations at its global business services center. Help improve financial close and ERP processes while working in English and French, German or Dutch.

Ochish