Senior CRA

ICON plc

. Lead clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement .

Posted 11/4/2026full-timeRemote • California • United StatesSenior💰 $110,520 - $138,150 per yearWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in clinical trial monitoring, regulatory compliance, and site management, with a strong focus on quality assurance and continuous improvement. Proven ability to build relationships and collaborate effectively with cross-functional teams and stakeholders.

Highest-signal resume keywords

Clinical Trial MonitoringGood Clinical Practice (GCP)Site ManagementData IntegrityOphthalmology Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Research AssociateRegulatory RequirementsMonitoring PracticesOrganizational SkillsProblem-Solving Skills

Soft Skills

Communication SkillsInterpersonal SkillsStakeholder ManagementInfluencing Skills

Tools & Technologies

Clinical Trial Software

Industry Keywords

Clinical Trial ProcessesSite PerformanceTrial ExecutionCross-Functional Collaboration

About the role

Key responsibilities & impact

Lead clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement
Monitor clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards
Conduct site visits to assess site performance, resolve issues, and provide support for successful trial execution
Collaborate with cross-functional teams to ensure timely and accurate data collection and reporting
Provide training and guidance to site staff and other CRAs
Build and maintain effective relationships with site personnel and stakeholders to facilitate smooth trial operations

Requirements

What you’ll need

Bachelor's degree in a relevant scientific discipline or healthcare-related field
Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements
Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools
Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment
Experience monitoring complex indication in Ophthalmology
Willingness to travel as required (approximately 60%)
Candidates must be located in California (Orange County/LA/Modesto)
Employment with ICON is contingent upon having the legal right to work in the country where the role is based

Benefits

Comp & perks

Competitive base salary and 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
Learning and development opportunities through structured training and career pathways