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 Site Manager II – China (Remote)

Lead clinical trial site management for ICON plc in China, supporting protocol compliance, data integrity, and effective study execution. The role covers site oversight and collaboration across Beijing and Shanghai.

Сипаттама

  • Lead technically complex clinical trial monitoring activities with an emphasis on quality improvement
  • Evaluate sites against study protocols, regulatory obligations, and Good Clinical Practice standards
  • Perform site visits to review performance, address issues, and support successful study delivery
  • Partner with cross-functional teams to maintain accurate, timely data collection and reporting
  • Train and coach site personnel and fellow Clinical Research Associates
  • Develop productive working relationships with site teams and other key stakeholders

Талаптар

  • Hold a bachelor's degree in a relevant scientific or healthcare discipline
  • Bring extensive Clinical Research Associate experience and a strong grasp of clinical trial operations and regulatory requirements
  • Demonstrate the ability to oversee multiple sites and projects while applying strong organization and problem-solving skills
  • Have advanced knowledge of monitoring methods, data integrity, and site management, plus proficiency with relevant clinical trial software and tools
  • Communicate effectively with stakeholders and use strong interpersonal and relationship-management skills to promote compliance in complex settings
  • Be prepared to travel as needed, approximately 60% of the time
  • Have the legal right to work in the country where the position is based

Артықшылықтар

  • Base salary with performance-linked incentives
  • Health and wellbeing programmes, including medical, dental, and vision coverage where applicable
  • Retirement and pension provisions
  • Life assurance and disability protection
  • Employee assistance services and wellbeing resources
  • Professional development through structured training and career progression pathways

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