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 Trial Manager - Mexico Remote

Lead end-to-end clinical trial delivery for ICON plc, including study oversight, enrollment, budgets, start-up, and regulatory compliance. Guide cross-functional teams and support successful outcomes across complex clinical research programs.

Сипаттама

  • Lead the planning, execution, and completion of clinical trials
  • Maintain compliance with study timelines, budgets, and regulatory requirements
  • Coordinate clinical trial delivery, resolve operational issues, and strengthen team capabilities
  • Manage the clinical budget and allocate resources efficiently
  • Create monitoring plans and tools to support effective study oversight
  • Train and mentor Clinical Research Associates (CRAs)
  • Drive participant enrollment and lead study start-up activities
  • Review trip reports and introduce corrective and preventive action plans when needed
  • Build effective working relationships with sponsors, vendors, and cross-functional teams
  • Provide strategic direction to support successful clinical trial outcomes

Талаптар

  • At least 4 years of Clinical Trial Management experience within a CRO or pharmaceutical organization
  • A bachelor's degree in health sciences, life sciences, or a related field
  • At least 10 years of relevant clinical trial management experience
  • Monitoring experience of 2 or more years is preferred
  • Experience supporting complex protocols, such as MASH/NASH, radiopharmaceutical, or other specialized therapeutic programs, is highly valued
  • Experience managing complex or global clinical trials is advantageous
  • Experience overseeing all trial components from start-up through database lock is preferred
  • This position is for experienced CTM professionals; entry-level CTM experience alone is insufficient
  • Willingness to travel approximately 25% as required
  • Legal authorization to work in the country where the role is based

Артықшылықтар

  • Competitive 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 pathways supporting learning and development

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