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.

Senior Clinical Research Associate – South Africa (Remote)

Senior Clinical Research Associate overseeing site monitoring and trial execution for ICON’s sponsor-dedicated research programs. The role focuses on protocol compliance, site performance, data quality, and regulatory standards.

Tavsif

  • Support sponsor-dedicated research programs using ICON’s global clinical expertise
  • Manage clinical trial activities in line with protocols, regulations, and industry standards
  • Lead technically complex monitoring work with a focus on quality and ongoing improvement
  • Evaluate site adherence to study protocols, regulatory requirements, and Good Clinical Practice standards
  • Conduct site visits to review performance, address issues, and help deliver trials successfully
  • Partner with cross-functional teams to support timely, accurate data collection and reporting
  • Train and advise site staff and fellow Clinical Research Associates
  • Develop relationships with site personnel and stakeholders to support efficient trial operations

Talablar

  • Bachelor’s degree in a relevant scientific or healthcare-related discipline
  • Extensive Clinical Research Associate experience with a strong grasp of clinical trial processes and regulatory requirements
  • Demonstrated ability to coordinate multiple sites and projects while applying strong organization and problem-solving skills
  • Advanced knowledge of monitoring methods, data integrity, and site management, including relevant clinical trial software and tools
  • Strong communication, interpersonal, and stakeholder management abilities, with the capacity to influence compliance in a complex environment
  • Availability to travel as needed, approximately 60% of the time
  • Legal authorization to work in the country where the role is located

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

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