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 Trial Manager II at ICON plc – Remote in Argentina

Lead clinical trial operations, data review, and regulatory compliance for ICON plc, a global clinical research organization. Coordinate cross-functional teams and study deliverables in a remote role based in Buenos Aires.

Tavsif

  • Manage clinical trial workstreams and ensure deliverables meet quality and timeline requirements
  • Partner with cross-functional teams to plan and execute effective participant enrollment strategies
  • Create and implement comprehensive clinical trial protocols with relevant internal teams
  • Direct daily clinical trial operations in accordance with applicable regulatory standards
  • Review and interpret trial data, identify trends, and recommend ways to improve study outcomes
  • Anticipate execution challenges and implement practical solutions to keep trials on track
  • Build effective relationships with internal and external stakeholders to support smooth trial delivery
  • Balance competing priorities while supporting team development

Talablar

  • Bachelor's degree in a relevant field
  • At least [X] years of experience managing clinical trials
  • Demonstrated expertise in clinical trial design and execution
  • Strong knowledge of applicable regulatory requirements
  • Advanced analytical and problem-solving abilities
  • Ability to interpret complex medical data
  • Clear and effective communication and interpersonal skills
  • Ability to work collaboratively across diverse teams
  • Strong attention to detail and organizational skills
  • Proven ability to manage multiple tasks and competing priorities successfully
  • Willingness to travel as needed, approximately 25%
  • Legal authorization to work in the country where the role is based

Imtiyozlar

  • Competitive base pay with performance-related incentives
  • Health and wellbeing programs, including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programs and wellbeing resources
  • Structured training and career development opportunities

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