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 Coordinator, Standards

Senior coordinator overseeing clinical trial data and standards for ICON’s sponsor-dedicated research programs. Supports data quality, compliance, reconciliation, and timely study delivery.

Сипаттама

  • Plan and assess clinical trials, interpret complex medical data, and support the development of new treatments and therapies.
  • Lead technically demanding clinical research activities, prioritizing quality and ongoing improvement.
  • Develop and maintain data management plans and study records in line with industry standards and regulatory requirements.
  • Find and resolve data inconsistencies to improve data flow and quality across the study lifecycle.
  • Work with clinical operations and biostatistics teams to design and carry out study-specific data management approaches.
  • Complete project work to keep studies on schedule, including filing and archiving records and sending queries to investigator sites.
  • Guide junior data coordinators in data reconciliation, coding, and cleaning practices.

Талаптар

  • Bachelor’s degree in a relevant discipline, such as life sciences or healthcare.
  • Demonstrated clinical data management experience in the pharmaceutical or biotechnology industry.
  • Familiarity with clinical data management tools such as Medidata, Oracle RDC, or similar systems.
  • Strong attention to detail and effectiveness in a fast-paced work environment.
  • Excellent communication and ability to work with cross-functional teams.
  • Knowledge of regulatory guidance and standards, such as ICH-GCP, is an advantage.
  • Willingness to travel as needed, approximately 5%.
  • Must have legal authorization to work in the country where the role is based; employment with ICON is conditional on this.

Артықшылықтар

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

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