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 - Turkey (Remote)

Senior Clinical Research Associate role at ICON plc supporting sponsor-dedicated clinical trials in Turkey. The position focuses on protocol compliance, site performance, data quality, and regulatory standards.

Tavsif

  • Manage clinical trial activities in line with protocols, regulations, and industry standards
  • Lead technically complex monitoring work with an emphasis on quality and continuous improvement
  • Assess clinical sites for compliance with study protocols, regulations, and Good Clinical Practice standards
  • Conduct site visits to evaluate performance, address issues, and support successful trial delivery
  • Work with cross-functional teams to ensure accurate, timely data collection and reporting
  • Train and guide site staff and fellow Clinical Research Associates
  • Develop stakeholder relationships that support efficient trial operations

Talablar

  • Bachelor’s degree in a relevant scientific or healthcare-related discipline
  • Extensive Clinical Research Associate experience with strong knowledge of trial processes and regulatory requirements
  • Demonstrated ability to oversee multiple sites and projects while applying strong organizational and problem-solving skills
  • Advanced knowledge of monitoring, data integrity, and site management, including relevant clinical trial software and tools
  • Strong communication, interpersonal, and stakeholder-management skills, with the ability to influence compliance in complex environments
  • 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-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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