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 Trial Coordinator

Support ICON’s sponsor-dedicated clinical research operations by helping monitor U.S. trial sites remotely. Assist with trial documentation, compliance, site reporting, and team coordination.

Tavsif

  • Help monitor clinical trial sites for compliance with study protocols, regulations, and Good Clinical Practice (GCP) guidelines.
  • Prepare site documents, enter data, and track site performance measures.
  • Coordinate with cross-functional colleagues to share information and resolve site issues.
  • Keep site activity records accurate and help prepare monitoring reports.
  • Take part in training to build clinical trial management knowledge and skills.
  • Work with the team and stakeholders to deliver high-quality clinical research.

Talablar

  • Hold a bachelor’s degree in a relevant area, such as life sciences, healthcare administration, or clinical research.
  • Experience in clinical research, site management, or a related administrative role is preferred but not required.
  • Have strong organizational skills and attention to detail, with the ability to manage several tasks effectively.
  • Knowledge of clinical trial processes and regulatory requirements is an advantage.
  • Bring strong communication and interpersonal skills and the ability to work well with a team.
  • Be willing to travel as needed, approximately 25% of the time.
  • Have legal authorization to work in the country where the role is based.

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 pathways for learning and development.