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, Remote Oncology Trials

Lead remote monitoring for Phase I oncology trials with ICON Strategic Solutions. Oversee sites, compliance, data quality, and CRA support.

Сипаттама

  • Direct clinical trial activities in line with protocols, regulations, and industry standards
  • Lead technically complex monitoring work with an emphasis on quality and ongoing improvement
  • Verify site compliance with study protocols, regulations, and Good Clinical Practice standards
  • Conduct site visits, evaluate performance, resolve issues, and support effective study delivery
  • Coordinate with cross-functional teams to ensure accurate, timely data collection and reporting
  • Train and mentor site staff and fellow Clinical Research Associates
  • Develop and sustain effective relationships with site teams and key stakeholders

Талаптар

  • Bachelor’s degree in a relevant scientific or healthcare-related discipline
  • Extensive Clinical Research Associate experience with strong knowledge of clinical trial processes and regulatory requirements
  • Demonstrated ability to manage multiple sites and projects while applying strong organization and problem-solving skills
  • Advanced knowledge of monitoring practices, data integrity, and site management, including relevant clinical trial software and tools
  • Strong communication, interpersonal, and stakeholder management abilities, with the capacity to promote compliance in complex environments
  • Willingness to travel approximately 60% as required
  • Current oncology monitoring experience
  • Legal authorization to work in the country where the role is based

Артықшылықтар

  • Competitive 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 pathways supporting learning and development

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