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 - Malaysia Remote

Lead clinical trial monitoring, site oversight, and compliance activities for ICON’s sponsor-dedicated research programs in Malaysia.

Сипаттама

  • Direct technically complex clinical trial monitoring activities while advancing quality and continuous improvement
  • Oversee trial sites for compliance with study protocols, regulatory standards, and Good Clinical Practice requirements
  • Perform site visits to evaluate performance, address issues, and support effective trial delivery
  • Partner with cross-functional teams to maintain accurate, timely data collection and reporting
  • Train and mentor site personnel and fellow Clinical Research Associates
  • Develop strong working relationships with site teams and stakeholders to support efficient trial operations

Талаптар

  • Bachelor’s degree in a relevant scientific or healthcare discipline
  • Substantial Clinical Research Associate experience with a strong command of clinical trial operations and regulatory requirements
  • 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, along with proficiency in applicable clinical trial systems and tools
  • Strong communication, interpersonal, and stakeholder management capabilities, including the ability to influence compliance in complex settings
  • Ability and willingness to travel approximately 60% as required
  • Legal authorization to work in the country where the position is based

Артықшылықтар

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

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