Senior Clinical Research Associate

ICON plc

Senior Clinical Research Associate overseeing clinical trial monitoring for ICON, a global healthcare intelligence and clinical research organisation. Managing sites, compliance, data integrity, and trial execution across the US.

Posted 8/5/2026full-timeRemote • Pennsylvania • 🇺🇸 United StatesSeniorWebsite

Core Competencies

Role fit

Core Competencies

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

Demonstrates expertise in managing clinical trial activities, ensuring compliance with regulatory requirements and Good Clinical Practice (GCP) standards. Proficient in site management, data integrity, and effective communication with stakeholders to facilitate successful trial execution.

Highest-signal resume keywords

Clinical Trial ManagementGood Clinical Practice (GCP)Site MonitoringData IntegrityStakeholder Management

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Clinical Trial ProcessesRegulatory RequirementsSite Performance AssessmentMonitoring PracticesProject Management

Soft Skills

Organizational SkillsProblem-Solving SkillsInterpersonal SkillsCommunication SkillsInfluencing Skills

Tools & Technologies

Clinical Trial Software

Industry Keywords

Clinical Research AssociateCross-Functional CollaborationTrial ExecutionData CollectionCompliance

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Oversee and manage clinical trial activities according to protocol, regulatory requirements, and industry standards
Lead clinical trial monitoring tasks requiring technical depth, 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 site performance, resolve issues, and support 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 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
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 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