ICON plc
ICON plc
ICON plc — денсаулық сақтау және фармацевтика салаларына қызмет көрсететін жаһандық келісімшарттық зерттеу ұйымы. Компанияның жұмысы бастапқы зерттеулерден бастап нарыққа шығарудан кейінгі қызметтерге дейін дәрі-дәрмек әзірлеуді қолдайтын клиникалық, консультациялық және коммерциялық қызметтерді қамтиды. ICON plc орталықтандырылмаған клиникалық зерттеулер, жүрек қауіпсіздігі, ерте клиникалық зертханалар, медициналық бейнелеу, реттеуші ақпарат және нақты өмір деректері сияқты шешімдер ұсынады. Сондай-ақ компания жүрек-қантамыр аурулары, онкология, ішкі аурулар, жасушалық және гендік терапиялар, биосимилярлар сияқты бағыттарда терапиялық тәжірибесін қолданып, клиникалық бағдарламалардың ілгерілеуіне көмектесу үшін деректерді талдауды пациентке бағдарланған тәсілдермен ұштастырады.

Senior Clinical Research Associate - Canada Remote

ICON plc is seeking a Senior Clinical Research Associate to monitor respiratory and cardiovascular trials across the Greater Toronto Area. The role oversees site performance, regulatory compliance, data quality, and trial delivery.

Сипаттама

  • Manage clinical trial activities in line with study protocols, regulations, and industry standards
  • Direct technically complex monitoring activities while advancing quality and continuous improvement
  • Evaluate site compliance with protocols, regulations, and Good Clinical Practice (GCP) requirements
  • Conduct site visits to review performance, address issues, and support effective trial delivery
  • Partner with cross-functional teams to maintain accurate, timely data collection and reporting
  • Train and support site personnel and fellow Clinical Research Associates
  • Develop productive relationships with site teams and stakeholders to support efficient trial operations
  • Monitor respiratory and cardiovascular studies throughout the Greater Toronto Area

Талаптар

  • Bachelor’s degree in a relevant scientific or healthcare-related discipline
  • Extensive Clinical Research Associate experience with a strong grasp of clinical trial processes and regulatory obligations
  • 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
  • Proficiency with relevant clinical trial software and tools
  • Strong communication, interpersonal, and stakeholder management capabilities, including the ability to influence compliance in complex settings
  • Availability to travel as needed, approximately 60%
  • Legal authorization to work in the country where the position is based

Артықшылықтар

  • Base salary with performance-based incentives
  • Health and wellbeing programmes, including medical, dental, and vision coverage where applicable
  • Retirement and pension programmes
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Structured training and career development opportunities

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