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 Associate - Spain (Remote) | ICON plc

Coordinate sponsor-dedicated clinical trials for ICON across global research programs. Maintain protocol compliance, site oversight, data quality, and timely study execution.

Сипаттама

  • Lead technically complex clinical coordination activities while advancing quality and continuous improvement
  • Coordinate trial operations to meet protocols, regulatory obligations, and delivery milestones
  • Partner with cross-functional teams to resolve study issues, improve processes, and support effective execution
  • Oversee site management and monitoring activities to protect data integrity and protocol compliance
  • Guide clinical staff and investigators on best practices and applicable regulatory standards
  • Monitor and communicate study progress, assess emerging risks, and apply mitigation strategies

Талаптар

  • Bachelor’s degree in a relevant scientific or healthcare discipline
  • Substantial clinical trial management experience with a sound grasp of study processes and regulatory obligations
  • Demonstrated ability to organize and deliver multiple projects while solving problems effectively
  • Strong communication and relationship-building skills for working with varied teams and stakeholders
  • Careful, proactive approach to supporting trial outcomes and resolving clinical issues
  • Legal authorization to work in the country of employment

Артықшылықтар

  • Base pay with performance-based incentives
  • Health and wellbeing support, including medical, dental, and vision coverage where applicable
  • Retirement and pension arrangements
  • Life assurance and disability protection
  • Employee assistance services and wellbeing resources
  • Structured training and career development opportunities

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