Senior Clinical Research Associate

ICON plc

. Lead clinical trial monitoring tasks with a focus on quality and continuous improvement .

Posted 9/24/2026full-timeRemote • United StatesSenior💰 $110,520 - $138,150 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical trial monitoring, ensuring adherence to protocols and regulatory requirements while fostering strong relationships with site personnel. Proficient in managing multiple projects and sites, with a focus on data integrity and compliance in the oncology field.

Highest-signal resume keywords

Clinical Trial MonitoringGood Clinical Practice (GCP)Data IntegritySite ManagementStakeholder Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ProcessesRegulatory RequirementsOncology KnowledgeSite Performance AssessmentProject Management

Soft Skills

Organizational SkillsProblem-Solving SkillsCommunication SkillsInterpersonal SkillsInfluencing Skills

Tools & Technologies

Clinical Trial Software

Industry Keywords

Clinical Research AssociateSponsor-Dedicated FSP ModelPhase I TrialsContinuous Improvement

About the role

Key responsibilities & impact

Lead clinical trial monitoring tasks with a focus on quality and continuous improvement
Monitor clinical trial sites for adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards
Conduct site visits to assess performance, resolve issues, and support successful trial execution
Collaborate with cross-functional teams on timely and accurate data collection and reporting
Provide training and guidance to site staff and other CRAs
Build and maintain relationships with site personnel and stakeholders
Work in a sponsor-dedicated FSP model with a focus on Oncology, preferably Phase I

Requirements

What you’ll need

Bachelor's degree in a relevant scientific discipline or healthcare-related field
Extensive experience as a Clinical Research Associate
Strong understanding of clinical trial processes and regulatory requirements
Proven ability to manage multiple sites and projects simultaneously
Strong organizational and problem-solving skills
Expertise in monitoring practices, data integrity, and site management
Proficiency in relevant clinical trial software and tools
Excellent communication, interpersonal, and stakeholder management skills
Ability to influence and drive compliance within a complex environment
Willingness to travel as required (approximately 60%)
Legal right to work in the country where the role is based

Benefits

Comp & perks

Competitive base salary
Performance related incentives
Medical coverage where applicable
Dental coverage where applicable
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