ICON plc
ICON plc
ICON plc is a global contract research organisation serving the healthcare and pharmaceutical industries. Its work spans clinical, consulting, and commercial services that support drug development from early research through post-marketing activities. The company provides solutions including decentralised clinical trials, cardiac safety, early clinical laboratories, medical imaging, regulatory intelligence, and real-world evidence. ICON plc also brings therapeutic expertise to areas such as cardiovascular disease, oncology, internal medicine, cell and gene therapies, and biosimilars, combining data analysis with patient-focused approaches to help advance clinical programmes.

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.

Description

  • 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

Requirements

  • 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

Benefits

  • 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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