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 – Beijing (Hybrid)

Lead site monitoring, compliance, and trial delivery for ICON plc’s sponsor-dedicated clinical research programs in China.

Tavsif

  • Direct clinical trial operations in line with study protocols, regulations, and industry standards
  • Take ownership of technically complex monitoring activities while advancing quality and continuous improvement
  • Verify that study sites follow protocols, regulatory obligations, and Good Clinical Practice (GCP) requirements
  • Visit sites to evaluate performance, address issues, and help keep trials on track
  • Partner with cross-functional teams to support accurate, timely data collection and reporting
  • Train and mentor site personnel and fellow Clinical Research Associates
  • Develop strong working relationships with investigators, site teams, and other stakeholders
  • Coordinate multiple sites and projects concurrently

Talablar

  • Bachelor’s degree in a relevant scientific or healthcare-related discipline
  • Substantial Clinical Research Associate experience, including a strong command of clinical trial processes and regulatory requirements
  • Demonstrated success managing several sites and projects at once, supported by strong organization and problem-solving abilities
  • Advanced knowledge of monitoring methods, data integrity, and site management, plus proficiency with applicable clinical trial software and tools
  • Strong communication, interpersonal, and stakeholder-management capabilities, with the ability to influence compliance in a complex setting
  • Availability to travel as needed, approximately 60% of the time
  • Legal authorization to work in the country where the position is located

Imtiyozlar

  • Competitive base pay with performance-based incentives
  • Health and wellbeing programs, including medical, dental, and vision coverage where applicable
  • Retirement and pension benefits
  • Life assurance and disability protection
  • Employee assistance programs and wellbeing resources
  • Professional development through structured training and career progression pathways

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