Senior Clinical Research Associate

ICON plc

. Work in a sponsor-dedicated model supported by ICON’s global expertise .

Posted 9/21/2026full-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 within the cardiovascular medical device sector, with a strong focus on A-fib studies. Proficient in FDA regulations, ICH/GCP guidelines, and effective communication strategies to foster relationships with site personnel and investigators.

Highest-signal resume keywords

Clinical Trial MonitoringCardiovascular Medical Device ExperienceFDA Regulations KnowledgeICH/GCP Guidelines FamiliarityStrong Problem-Solving Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Monitoring ExperienceReport PreparationRisk MitigationClinical Trial ManagementDetail-Oriented Analysis

Soft Skills

Interpersonal SkillsEffective CommunicationAbility to Manage Multiple PrioritiesIndependent Work Capability

Industry Keywords

CardiovascularElectrophysiologyA-fibClinical TrialsLife SciencePhysical ScienceNursingBiological Science

About the role

Key responsibilities & impact

Work in a sponsor-dedicated model supported by ICON’s global expertise
Support one study in the cardiovascular/electrophysiology medical device space focused on A-fib
Monitor clinical trial sites and identify and mitigate risks
Establish and maintain working relationships with site personnel, investigators, and internal teams
Communicate effectively with study teams and sites using a well-executed communication plan
Manage multiple priorities in a dynamic environment
Prepare rigorous, detail-oriented, and precise reports
Cover the Central/West region with up to 65% regional travel

Requirements

What you’ll need

3 years of monitoring experience required
A bachelor’s degree is required, preferably a Bachelor of Science Degree in Life Science, Physical Science, Nursing or Biological Science
Cardiovascular medical device monitoring experience preferred; complex cardiovascular/electrophysiology pharma monitoring and/or Coordinator/Nursing experience considered
In-depth knowledge of FDA regulations and ICH/GCP guidelines
Strong problem-solving skills to mitigate risks and identify issues at sites and implement effective solutions promptly
Strong interpersonal skills to establish and maintain effective working relationships with site personnel, investigators, and internal teams
Exceptional verbal and written communication skills
Ability to tailor communication style to different stakeholders
Ability to work independently and manage multiple priorities
Well-versed in clinical trial management
Located in the West region in the US near a major airport
Ability to cover up to 65% regional travel
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
Up to 65% regional travel coverage