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 Data Manager, Data Standards

Lead clinical data standards, quality, and governance for ICON’s sponsor-dedicated trials. Improve global processes and coordinate delivery across teams.

Сипаттама

  • Lead the development and implementation of clinical data standards processes and best practices.
  • Drive work on data cleaning, data quality, edit checks, data listings, and standards library management.
  • Work closely with Clinical Trial Reporting (CTR), Clinical Trial Configuration (CTC), and Cross-Functional Data Review (CFDR) teams.
  • Set governance, workflows, and quality standards that support clinical trial delivery.
  • Lead and mentor Associate Manager-level colleagues and encourage continuous improvement.
  • Work with cross-functional stakeholders to turn strategic objectives into operational plans.
  • Identify risks, improve processes, and advance data quality throughout the clinical data lifecycle.

Талаптар

  • Hold a bachelor’s degree in life sciences, health sciences, or a related field.
  • Bring extensive clinical data management experience from a CRO, biotechnology, or pharmaceutical setting.
  • Have strong experience in process development, project management, stakeholder engagement, and cross-functional collaboration.
  • Show a proven ability to build and implement new processes and ways of working.
  • Have experience with data quality, standards development, data review, edit checks, data listings, or standards library management.
  • Understand clinical trial processes, regulatory requirements, and ICH-GCP.
  • Demonstrate strong communication, problem-solving, and leadership skills.
  • Bring an entrepreneurial outlook and the ability to thrive in a developing, evolving function.
  • Have legal authorization to work in the country where the role is based.

Артықшылықтар

  • Competitive base pay with performance-related incentives.
  • Health and wellbeing programmes, including medical, dental, and vision coverage where applicable.
  • Retirement and pension plans.
  • Life assurance and disability coverage.
  • Employee assistance programmes and wellbeing resources.
  • Learning and development through structured training and career pathways.

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