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 Site Manager II – China (Remote)

Lead clinical trial site management for ICON plc in China, supporting protocol compliance, data integrity, and effective study execution. The role covers site oversight and collaboration across Beijing and Shanghai.

Tavsif

  • Lead technically complex clinical trial monitoring activities with an emphasis on quality improvement
  • Evaluate sites against study protocols, regulatory obligations, and Good Clinical Practice standards
  • Perform site visits to review performance, address issues, and support successful study delivery
  • Partner with cross-functional teams to maintain accurate, timely data collection and reporting
  • Train and coach site personnel and fellow Clinical Research Associates
  • Develop productive working relationships with site teams and other key stakeholders

Talablar

  • Hold a bachelor's degree in a relevant scientific or healthcare discipline
  • Bring extensive Clinical Research Associate experience and a strong grasp of clinical trial operations and regulatory requirements
  • Demonstrate the ability to oversee multiple sites and projects while applying strong organization and problem-solving skills
  • Have advanced knowledge of monitoring methods, data integrity, and site management, plus proficiency with relevant clinical trial software and tools
  • Communicate effectively with stakeholders and use strong interpersonal and relationship-management skills to promote compliance in complex settings
  • Be prepared to travel as needed, approximately 60% of the time
  • Have the legal right to work in the country where the position is based

Imtiyozlar

  • Base salary with performance-linked incentives
  • Health and wellbeing programmes, including medical, dental, and vision coverage where applicable
  • Retirement and pension provisions
  • Life assurance and disability protection
  • Employee assistance services and wellbeing resources
  • Professional development through structured training and career progression pathways

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