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, Oncology Trials — Romania

Monitor oncology clinical trials remotely in Romania for ICON’s sponsor-dedicated research services. Oversee study sites, compliance, data quality, and trial delivery.

Сипаттама

  • Manage clinical trial activities in line with study protocols, regulations, and industry standards.
  • Lead technically complex monitoring work, emphasizing quality and ongoing improvement.
  • Check that trial sites follow study protocols, regulatory requirements, and Good Clinical Practice (GCP).
  • Visit sites to evaluate performance, address issues, and support effective trial delivery.
  • Work with cross-functional teams to ensure data is collected and reported accurately and on time.
  • Train and advise site staff and fellow Clinical Research Associates.
  • Build productive relationships with site teams and stakeholders to support efficient trial operations.

Талаптар

  • Bachelor’s degree in a relevant science or healthcare field.
  • Substantial Clinical Research Associate experience and a strong grasp of clinical trial procedures and regulatory requirements.
  • Previous on-site monitoring experience with oncology trials.
  • Expert knowledge of monitoring, data integrity, and site management, plus proficiency with relevant clinical trial software and tools.
  • Strong communication, interpersonal, and stakeholder management abilities, including the capacity to influence and promote compliance in a complex setting.
  • Available to travel as needed, approximately 60%.
  • Authorized to work legally in Romania.

Артықшылықтар

  • Competitive base pay with performance 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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