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 Associate - Spain (Remote) | ICON plc

Coordinate sponsor-dedicated clinical trials for ICON across global research programs. Maintain protocol compliance, site oversight, data quality, and timely study execution.

Tavsif

  • Lead technically complex clinical coordination activities while advancing quality and continuous improvement
  • Coordinate trial operations to meet protocols, regulatory obligations, and delivery milestones
  • Partner with cross-functional teams to resolve study issues, improve processes, and support effective execution
  • Oversee site management and monitoring activities to protect data integrity and protocol compliance
  • Guide clinical staff and investigators on best practices and applicable regulatory standards
  • Monitor and communicate study progress, assess emerging risks, and apply mitigation strategies

Talablar

  • Bachelor’s degree in a relevant scientific or healthcare discipline
  • Substantial clinical trial management experience with a sound grasp of study processes and regulatory obligations
  • Demonstrated ability to organize and deliver multiple projects while solving problems effectively
  • Strong communication and relationship-building skills for working with varied teams and stakeholders
  • Careful, proactive approach to supporting trial outcomes and resolving clinical issues
  • Legal authorization to work in the country of employment

Imtiyozlar

  • Base pay with performance-based incentives
  • Health and wellbeing support, including medical, dental, and vision coverage where applicable
  • Retirement and pension arrangements
  • Life assurance and disability protection
  • Employee assistance services and wellbeing resources
  • Structured training and career development opportunities

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