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ICON plc
ICON plc
KonsultavimasLogistikaSveikatos priežiūra
ICON plc yra pasaulinė sutartinių tyrimų organizacija, teikianti paslaugas sveikatos priežiūros ir farmacijos sektoriams. Jos veikla apima klinikines, konsultavimo ir komercines paslaugas, padedančias vykdyti vaistų kūrimą nuo ankstyvųjų tyrimų iki veiklos po pateikimo į rinką. Įmonė teikia decentralizuotų klinikinių tyrimų, širdies saugumo vertinimo, ankstyvosios klinikinės laboratorinės veiklos, medicininio vaizdinimo, reguliacinės žvalgybos ir realaus pasaulio įrodymų sprendimus. ICON plc taip pat turi terapinių sričių kompetencijos, įskaitant širdies ir kraujagyslių ligas, onkologiją, vidaus ligas, ląstelių ir genų terapijas bei biologiškai panašius vaistus. Derindama duomenų analizę su į pacientą orientuotais metodais, įmonė padeda plėtoti klinikines programas.
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Darbai įmonėje

Clinical Research Associate – Respiratory and Cardiovascular Trials, Canada Remote

Monitor respiratory and cardiovascular clinical trials for ICON’s sponsor-dedicated research operations. Oversee GTA sites, compliance, data quality, and trial delivery.

CAKanadaNuotolinisVisas etatasJaunesnysis specialistasVidutinis lygisPrivaloma Kalba: anglųKlinikiniai tyrimai

Aprašymas

  • Manage clinical trial activities in line with protocols, regulations, and industry standards
  • Lead monitoring activities with an emphasis on quality and ongoing improvement
  • Verify site compliance with study protocols, regulations, and Good Clinical Practice standards
  • Conduct site visits to evaluate performance, resolve concerns, and provide operational support
  • Coordinate with cross-functional teams to ensure accurate, timely data collection and reporting
  • Train and mentor site personnel and fellow Clinical Research Associates
  • Develop and maintain effective relationships with site teams and key stakeholders
  • Monitor respiratory and cardiovascular studies across the GTA

Reikalavimai

  • Bachelor’s degree in a relevant scientific discipline or healthcare-related field
  • Extensive Clinical Research Associate experience, with a strong grasp of clinical trial procedures and regulatory requirements
  • Demonstrated ability to manage multiple sites and projects concurrently, supported by strong organizational and problem-solving skills
  • Advanced knowledge of monitoring methods, data integrity, and site management
  • Proficiency with relevant clinical trial software and tools
  • Strong communication, interpersonal, and stakeholder management capabilities
  • Ability to influence others and promote compliance in a complex environment
  • Willingness to travel as needed, approximately 60%
  • Legal authorization to work in the country where the role is based

Privalumai

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

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