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.

Clinical Trial Manager II at ICON plc – Remote in Argentina

Lead clinical trial operations, data review, and regulatory compliance for ICON plc, a global clinical research organization. Coordinate cross-functional teams and study deliverables in a remote role based in Buenos Aires.

Сипаттама

  • Manage clinical trial workstreams and ensure deliverables meet quality and timeline requirements
  • Partner with cross-functional teams to plan and execute effective participant enrollment strategies
  • Create and implement comprehensive clinical trial protocols with relevant internal teams
  • Direct daily clinical trial operations in accordance with applicable regulatory standards
  • Review and interpret trial data, identify trends, and recommend ways to improve study outcomes
  • Anticipate execution challenges and implement practical solutions to keep trials on track
  • Build effective relationships with internal and external stakeholders to support smooth trial delivery
  • Balance competing priorities while supporting team development

Талаптар

  • Bachelor's degree in a relevant field
  • At least [X] years of experience managing clinical trials
  • Demonstrated expertise in clinical trial design and execution
  • Strong knowledge of applicable regulatory requirements
  • Advanced analytical and problem-solving abilities
  • Ability to interpret complex medical data
  • Clear and effective communication and interpersonal skills
  • Ability to work collaboratively across diverse teams
  • Strong attention to detail and organizational skills
  • Proven ability to manage multiple tasks and competing priorities successfully
  • Willingness to travel as needed, approximately 25%
  • Legal authorization to work in the country where the role is based

Артықшылықтар

  • Competitive base pay 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 development opportunities

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