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 Trial Associate – Hybrid, Mannheim

Support clinical trial administration and operational delivery for ICON’s sponsor-dedicated pharmaceutical services. Coordinate regulatory documentation, site communications, trial records, and stakeholder activities.

Tavsif

  • Support clinical trials through documentation management, meeting coordination, and accurate maintenance of trial records
  • Prepare and submit regulatory documentation while maintaining alignment with study protocols and applicable requirements
  • Partner with cross-functional teams to advance trial operations and address issues arising during the study
  • Track study progress, coordinate site communications, and help ensure study materials are delivered on schedule
  • Develop effective working relationships with site personnel and other stakeholders to support efficient trial delivery
  • Own assigned clinical trial management deliverables and use specialist knowledge to address complex operational challenges

Talablar

  • Bachelor’s degree in a relevant scientific or healthcare-related discipline
  • Substantial experience supporting clinical trials, with a sound understanding of trial processes and regulatory requirements
  • Highly organized, able to prioritize and manage multiple tasks and projects effectively
  • Experience with clinical trial management systems and related software, with strong attention to documentation and data accuracy
  • Strong communication, interpersonal, and problem-solving abilities, along with the capacity to collaborate with varied teams and stakeholders
  • Willingness to travel as needed, approximately 10%
  • Fluency in German and English
  • Legal authorization to work in the country where the position is based

Imtiyozlar

  • 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 development opportunities

O‘xshash ish o‘rinlari