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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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Darbai įmonėje

Senior Clinical Research Associate, Oncology Trials — Romania

Monitor oncology clinical trials remotely in Romania for ICON’s sponsor-dedicated research services. Oversee study sites, compliance, data quality, and trial delivery.

RORumunijaNuotolinisVisas etatasVyresnysis specialistasPrivaloma Kalba: anglųKlinikiniai tyrimai
Google Cloud Platform

Aprašymas

  • Manage clinical trial activities in line with study protocols, regulations, and industry standards.
  • Lead technically complex monitoring work, emphasizing quality and ongoing improvement.
  • Check that trial sites follow study protocols, regulatory requirements, and Good Clinical Practice (GCP).
  • Visit sites to evaluate performance, address issues, and support effective trial delivery.
  • Work with cross-functional teams to ensure data is collected and reported accurately and on time.
  • Train and advise site staff and fellow Clinical Research Associates.
  • Build productive relationships with site teams and stakeholders to support efficient trial operations.

Reikalavimai

  • Bachelor’s degree in a relevant science or healthcare field.
  • Substantial Clinical Research Associate experience and a strong grasp of clinical trial procedures and regulatory requirements.
  • Previous on-site monitoring experience with oncology trials.
  • Expert knowledge of monitoring, data integrity, and site management, plus proficiency with relevant clinical trial software and tools.
  • Strong communication, interpersonal, and stakeholder management abilities, including the capacity to influence and promote compliance in a complex setting.
  • Available to travel as needed, approximately 60%.
  • Authorized to work legally in Romania.

Privalumai

  • Competitive base pay with performance 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

Lucis (YC X25)

Customer Care Specialist, Paris Hybrid

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1 – 10 Darbuotojai
Dirbtinis intelektasGera savijautaSveikatos priežiūra
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IT Support Specialist

Seeders
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2 750 € – 3 250 € / mėnuo
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DMI (Digital Management, LLC)

Service Desk Analyst (Remote, United States) at DMI

DMI (Digital Management, LLC)
1 001 – 5 000 Darbuotojai
KonsultavimasLogistikaSveikatos priežiūra
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NuotolinisVisas etatasJaunesnysis specialistasDiplomas nebūtinasPrivaloma Kalba: anglųAnalitikas

Serve as the first point of contact for federal application users, resolving routine support issues and routing complex tickets. Support DMI’s managed IT services operation.

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Medavie

Bilingual Customer Service Representative (Remote, Canada)

Medavie
5 001 – 10 000 Darbuotojai
Bendruomenės sveikataSveikatos draudimasSveikatos priežiūra
CAKanada
40 254 $ – 45 285 $ / metai
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