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 Manager - Mexico Remote

Lead end-to-end clinical trial delivery for ICON plc, including study oversight, enrollment, budgets, start-up, and regulatory compliance. Guide cross-functional teams and support successful outcomes across complex clinical research programs.

Tavsif

  • Lead the planning, execution, and completion of clinical trials
  • Maintain compliance with study timelines, budgets, and regulatory requirements
  • Coordinate clinical trial delivery, resolve operational issues, and strengthen team capabilities
  • Manage the clinical budget and allocate resources efficiently
  • Create monitoring plans and tools to support effective study oversight
  • Train and mentor Clinical Research Associates (CRAs)
  • Drive participant enrollment and lead study start-up activities
  • Review trip reports and introduce corrective and preventive action plans when needed
  • Build effective working relationships with sponsors, vendors, and cross-functional teams
  • Provide strategic direction to support successful clinical trial outcomes

Talablar

  • At least 4 years of Clinical Trial Management experience within a CRO or pharmaceutical organization
  • A bachelor's degree in health sciences, life sciences, or a related field
  • At least 10 years of relevant clinical trial management experience
  • Monitoring experience of 2 or more years is preferred
  • Experience supporting complex protocols, such as MASH/NASH, radiopharmaceutical, or other specialized therapeutic programs, is highly valued
  • Experience managing complex or global clinical trials is advantageous
  • Experience overseeing all trial components from start-up through database lock is preferred
  • This position is for experienced CTM professionals; entry-level CTM experience alone is insufficient
  • Willingness to travel approximately 25% 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 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 pathways supporting learning and development

O‘xshash ish o‘rinlari

Kreato Global | BPO and Language Solutions

Remote English-Spanish OPI/VRI Interpreter

Kreato Global | BPO and Language Solutions

Interpret remotely between English- and Spanish-speaking people in medical, financial, social service, and customer care settings. Provide language support for Kreato Global across Latin America.

Ochish