Senior Clinical Research Associate, Medical Device

ICON plc

. Oversee and manage clinical trial activities according to protocol, regulatory requirements, and industry standards .

Posted 10/9/2026full-timeRemote • United StatesSenior💰 $110,520 - $138,150 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical trial activities, ensuring adherence to protocols and regulatory requirements while fostering collaboration across teams. Proficient in monitoring practices and site management, with a strong focus on data integrity and quality improvement.

Highest-signal resume keywords

Clinical Trial ManagementCRA Monitoring ExperienceGood Clinical Practice (GCP)Data IntegrityStakeholder Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ProcessesProtocol ManagementSite Performance AssessmentRegulatory RequirementsMonitoring PracticesData CollectionProject ManagementClinical Research Associate ExpertiseComplex Protocols ManagementClinical Trial Software Proficiency

Soft Skills

Communication SkillsInterpersonal SkillsTeam CollaborationTraining and GuidanceRelationship Building

Industry Keywords

CROPharmaClinical TrialsSite ManagementRegulatory Compliance

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 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
Manage multiple sites and projects simultaneously

Requirements

What you’ll need

Bachelor's degree in a relevant scientific discipline or healthcare-related field
3-5 years of CRA monitoring experience in CRO/pharma environments
Strong CRA experience managing complex protocols
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
Expertise in monitoring practices, data integrity, and site management
Proficiency in relevant clinical trial software and tools
Excellent communication, interpersonal, and stakeholder management skills
Willingness to travel as required (approximately 60%)
Limited Canadian travel may be required
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