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 – South Africa (Remote)

Senior Clinical Research Associate overseeing site monitoring and trial execution for ICON’s sponsor-dedicated research programs. The role focuses on protocol compliance, site performance, data quality, and regulatory standards.

Сипаттама

  • Support sponsor-dedicated research programs using ICON’s global clinical expertise
  • Manage clinical trial activities in line with protocols, regulations, and industry standards
  • Lead technically complex monitoring work with a focus on quality and ongoing improvement
  • Evaluate site adherence to study protocols, regulatory requirements, and Good Clinical Practice standards
  • Conduct site visits to review performance, address issues, and help deliver trials successfully
  • Partner with cross-functional teams to support timely, accurate data collection and reporting
  • Train and advise site staff and fellow Clinical Research Associates
  • Develop relationships with site personnel and stakeholders to support efficient trial operations

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 requirements
  • Demonstrated ability to coordinate multiple sites and projects while applying strong organization and problem-solving skills
  • Advanced knowledge of monitoring methods, data integrity, and site management, including relevant clinical trial software and tools
  • Strong communication, interpersonal, and stakeholder management abilities, with the capacity to influence compliance in a complex environment
  • Availability to travel as needed, approximately 60% of the time
  • Legal authorization to work in the country where the role is located

Артықшылықтар

  • Base salary with performance-related 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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