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ICON plc
ICON plc
KonsultavimasLogistikaSveikatos priežiūra
ICON plc yra pasaulinė sutartinių tyrimų organizacija, teikianti paslaugas sveikatos priežiūros ir farmacijos sektoriams. Jos veikla apima klinikines, konsultavimo ir komercines paslaugas, padedančias vykdyti vaistų kūrimą nuo ankstyvųjų tyrimų iki veiklos po pateikimo į rinką. Įmonė teikia decentralizuotų klinikinių tyrimų, širdies saugumo vertinimo, ankstyvosios klinikinės laboratorinės veiklos, medicininio vaizdinimo, reguliacinės žvalgybos ir realaus pasaulio įrodymų sprendimus. ICON plc taip pat turi terapinių sričių kompetencijos, įskaitant širdies ir kraujagyslių ligas, onkologiją, vidaus ligas, ląstelių ir genų terapijas bei biologiškai panašius vaistus. Derindama duomenų analizę su į pacientą orientuotais metodais, įmonė padeda plėtoti klinikines programas.
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Clinical Research Associate, Canada Remote

Monitor respiratory and cardiovascular clinical trials for ICON across the Greater Toronto Area. Support GCP compliance through site oversight, study visits, data integrity, and stakeholder guidance.

CAKanadaNuotolinisVisas etatasJaunesnysis specialistasVidutinis lygisPrivaloma Kalba: anglųKlinikiniai tyrimai
Google Cloud Platform

Aprašymas

  • Manage clinical trial activities in line with study protocols, regulations, and industry standards
  • Lead monitoring activities with an emphasis on quality and ongoing improvement
  • Assess clinical sites for compliance with protocols, regulations, and GCP requirements
  • Conduct site visits to evaluate performance, address issues, and support effective study delivery
  • Partner with cross-functional teams to ensure accurate, timely data collection and reporting
  • Train and advise site staff and fellow Clinical Research Associates
  • Develop and maintain effective relationships with site personnel and other stakeholders
  • Monitor respiratory and cardiovascular studies across the Greater Toronto Area

Reikalavimai

  • Bachelor’s degree in a relevant scientific or healthcare-related field
  • Substantial Clinical Research Associate experience and a strong understanding of clinical trial processes and regulatory requirements
  • Demonstrated ability to manage multiple sites and projects concurrently
  • Strong organizational and problem-solving capabilities
  • Advanced knowledge of monitoring practices, data integrity, and site management
  • Proficiency with relevant clinical trial software and tools
  • Excellent communication, interpersonal, and stakeholder management skills
  • Ability to influence others and promote compliance in a complex environment
  • Willingness to travel as needed, approximately 60%
  • Legal authorization to work in the country where the role is based

Privalumai

  • Base salary with performance-based 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

Susiję darbai

Terumo Medical Corporation

Region Manager, Terumo Interventional Systems Sales

Terumo Medical Corporation
1 001 – 5 000 Darbuotojai
H1B vizos rėmėjasGamybaKonsultavimasSveikatos priežiūra
USJungtinės ValstijosNJNaujasis Džersis
120 000 $ – 165 000 $ / metai
Darbas vietojeVisas etatasVidutinis lygisVyresnysis specialistasPrivaloma Kalba: anglųVadovas

Lead medical device sales across a North Central New Jersey region, managing field teams and hospital relationships. Drive regional revenue, sales performance, and compliant promotion of Terumo Interventional Systems products.

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