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 Associate at ICON plc - Pennsylvania Remote

Support clinical trial planning, coordination, monitoring, and close-out activities as a Clinical Associate at ICON plc. Contribute to sponsor-dedicated CRO services and the development of innovative treatments.

Tavsif

  • Support the planning, execution, and monitoring of clinical trials while maintaining compliance with protocols, regulations, and industry standards.
  • Coordinate study activities such as site initiation, patient recruitment, data collection, and monitoring visits.
  • Work cross-functionally with Clinical Operations, Data Management, and Biometrics teams.
  • Maintain complete study documentation and records in line with regulations and standard operating procedures.
  • Assist with study close-out, including data cleaning, analysis, and clinical study report preparation.

Talablar

  • Bachelor’s degree in a relevant scientific discipline or healthcare-related field.
  • Prior clinical research or healthcare experience, preferably in the pharmaceutical, biotechnology, or CRO sector.
  • Strong organizational and time-management abilities, including the capacity to prioritize competing tasks effectively.
  • Exceptional attention to detail and problem-solving skills, with a focus on data accuracy, integrity, and compliance.
  • Clear communication and strong interpersonal skills for collaborating across functions and building relationships with study teams and clinical sites.
  • Availability to travel as required.
  • Legal authorization to work in the country where the role is based.

Imtiyozlar

  • Competitive base salary with performance-related incentives.
  • Health and wellbeing programmes, including medical, dental, and vision coverage where applicable.
  • Retirement and pension plans.
  • Life assurance and disability coverage.
  • Employee assistance programmes and wellbeing resources.
  • Structured training and career pathways supporting learning and professional development.

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