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.

Clinical Research Associate, Canada Remote

Monitor respiratory and cardiovascular clinical trials for ICON across the Greater Toronto Area. Support GCP compliance through site oversight, study visits, data integrity, and stakeholder guidance.

Сипаттама

  • Manage clinical trial activities in line with study protocols, regulations, and industry standards
  • Lead monitoring activities with an emphasis on quality and ongoing improvement
  • Assess clinical sites for compliance with protocols, regulations, and GCP requirements
  • Conduct site visits to evaluate performance, address issues, and support effective study delivery
  • Partner with cross-functional teams to ensure accurate, timely data collection and reporting
  • Train and advise site staff and fellow Clinical Research Associates
  • Develop and maintain effective relationships with site personnel and other stakeholders
  • Monitor respiratory and cardiovascular studies across the Greater Toronto Area

Талаптар

  • Bachelor’s degree in a relevant scientific or healthcare-related field
  • Substantial Clinical Research Associate experience and a strong understanding of clinical trial processes and regulatory requirements
  • Demonstrated ability to manage multiple sites and projects concurrently
  • Strong organizational and problem-solving capabilities
  • Advanced knowledge of monitoring practices, data integrity, and site management
  • Proficiency with relevant clinical trial software and tools
  • Excellent communication, interpersonal, and stakeholder management skills
  • 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

Артықшылықтар

  • Base salary with performance-based 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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