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ICON plc
ICON plc
ConsultingHealthcareLogistics
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.
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Senior Clinical Research Associate – California Remote

Lead Phase I oncology trial monitoring for ICON’s sponsor-dedicated research programs. Oversee sites, compliance, data integrity, and clinical research associate guidance.

USUnited StatesCACalifornia
$110,520 – $138,150 / year
RemoteFull-timeSeniorEnglish RequiredClinical Research
Google Cloud Platform

Description

  • Manage clinical trial activities in line with protocols, regulations, and industry standards
  • Lead technically complex monitoring work focused on quality and continuous improvement
  • Assess site compliance with study protocols, regulations, and Good Clinical Practice standards
  • Conduct site visits to evaluate performance, resolve issues, and support trial delivery
  • Partner with cross-functional teams to ensure accurate, timely data collection and reporting
  • Train and support site staff and other clinical research associates
  • Maintain effective working relationships with site personnel and study 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 organizational and problem-solving skills
  • Advanced knowledge of monitoring practices, data integrity, and site management, including relevant clinical trial software and tools
  • Excellent communication, interpersonal, and stakeholder management abilities, with the capacity to influence 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 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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