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ICON plc
ICON plc
Asistență medicalăConsultanțăLogistică
ICON plc este o organizație globală de cercetare în regim contractual, care deservește industriile din domeniul sănătății și farmaceutic. Activitatea sa cuprinde servicii clinice, de consultanță și comerciale care sprijină dezvoltarea medicamentelor, de la cercetarea timpurie până la activitățile post-comercializare. Compania oferă soluții precum studii clinice descentralizate, evaluarea siguranței cardiace, laboratoare clinice pentru etapele timpurii, imagistică medicală, informații de reglementare și dovezi din lumea reală. ICON plc dispune, de asemenea, de expertiză terapeutică în domenii precum bolile cardiovasculare, oncologia, medicina internă, terapiile celulare și genice și medicamentele biosimilare, combinând analiza datelor cu o abordare axată pe pacienți pentru a contribui la avansarea programelor clinice.
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Locurile de muncă ale companiei

Senior Clinical Research Associate, Remote Oncology Trials

Lead remote monitoring for Phase I oncology trials with ICON Strategic Solutions. Oversee sites, compliance, data quality, and CRA support.

USStatele Unite ale AmericiiNCCarolina de NordTXTexasRemoteNormă întreagăSeniorLimbă Obligatorie: englezăCercetare clinică
Google Cloud Platform

Descriere

  • Direct clinical trial activities in line with protocols, regulations, and industry standards
  • Lead technically complex monitoring work with an emphasis on quality and ongoing improvement
  • Verify site compliance with study protocols, regulations, and Good Clinical Practice standards
  • Conduct site visits, evaluate performance, resolve issues, and support effective study delivery
  • Coordinate with cross-functional teams to ensure accurate, timely data collection and reporting
  • Train and mentor site staff and fellow Clinical Research Associates
  • Develop and sustain effective relationships with site teams and key stakeholders

Cerințe

  • Bachelor’s degree in a relevant scientific or healthcare-related discipline
  • Extensive Clinical Research Associate experience with strong knowledge of clinical trial processes and regulatory requirements
  • Demonstrated ability to manage multiple sites and projects while applying strong organization and problem-solving skills
  • Advanced knowledge of monitoring practices, data integrity, and site management, including relevant clinical trial software and tools
  • Strong communication, interpersonal, and stakeholder management abilities, with the capacity to promote compliance in complex environments
  • Willingness to travel approximately 60% as required
  • Current oncology monitoring experience
  • Legal authorization to work in the country where the role is based

Beneficii

  • Competitive base salary with performance-related incentives
  • Health and wellbeing programmes, including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Structured training and career pathways supporting learning and development

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