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 Research Associate - Malaysia Remote

Lead clinical trial monitoring, site oversight, and compliance activities for ICON’s sponsor-dedicated research programs in Malaysia.

Tavsif

  • Direct technically complex clinical trial monitoring activities while advancing quality and continuous improvement
  • Oversee trial sites for compliance with study protocols, regulatory standards, and Good Clinical Practice requirements
  • Perform site visits to evaluate performance, address issues, and support effective trial delivery
  • Partner with cross-functional teams to maintain accurate, timely data collection and reporting
  • Train and mentor site personnel and fellow Clinical Research Associates
  • Develop strong working relationships with site teams and stakeholders to support efficient trial operations

Talablar

  • Bachelor’s degree in a relevant scientific or healthcare discipline
  • Substantial Clinical Research Associate experience with a strong command of clinical trial operations and regulatory requirements
  • Demonstrated ability to oversee multiple sites and projects while applying strong organization and problem-solving skills
  • Advanced knowledge of monitoring methods, data integrity, and site management, along with proficiency in applicable clinical trial systems and tools
  • Strong communication, interpersonal, and stakeholder management capabilities, including the ability to influence compliance in complex settings
  • Ability and willingness to travel approximately 60% as required
  • Legal authorization to work in the country where the position is based

Imtiyozlar

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

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