Clinical Research Associate

ICON plc

. Work on multiple trials across cross-therapeutic areas with a start-up focus .

Posted 9/21/2026full-timeRemote • United StatesJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical trial start-up activities, ensuring compliance with ICH-GCP and local regulations, and effectively collaborating with site personnel and study teams. Proficient in utilizing clinical trial management systems and analytical tools to monitor site performance and drive patient recruitment strategies.

Highest-signal resume keywords

Clinical Trial ManagementGood Clinical Practice (GCP)Site Qualification VisitsRegulatory Document ManagementPatient Recruitment Strategies

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial MonitoringAnalytical MonitoringSite SelectionRegulatory ComplianceDocumentation Management

Soft Skills

Strong CommunicationInfluencing SkillsTeam CollaborationSelf-Starter

Tools & Technologies

CTMSEDCETMFIWRSDashboards/Metrics

Industry Keywords

Pharmaceutical IndustryCross-Therapeutic AreasInspection ReadinessStudy TimelinesLocal Regulatory Requirements

About the role

Key responsibilities & impact

Work on multiple trials across cross-therapeutic areas with a start-up focus
Collaborate with country operations teams to identify, select, and activate clinical trial sites
Perform Site Qualification Visits to assess site eligibility
Build relationships with site personnel to facilitate onboarding
Ensure activities comply with ICH-GCP, local regulations, and internal SOPs
Coordinate collection of regulatory approvals, contracts, and essential documents
Serve as the main point of contact for sites, study teams, and external stakeholders during start-up
Manage investigator contracts, regulatory documents, and site-specific start-up activities
Provide status updates aligned with project milestones
Monitor, report, and analyze KPIs related to site selection and start-up timelines
Identify and address issues that may delay study initiation or affect deliverables
Maintain accurate documentation for inspection readiness
Support sites through activation until Green Light status
Coordinate completion of pre-study requirements including contracts, budgets, and essential documentation
Assist with audit and inspection preparations

Requirements

What you’ll need

Minimum of a B.S., R.N., or equivalent degree, preferably in Biological Sciences
Preferred location is Nashville, TN; near a major airport; TN/KY near major hub acceptable
Minimum of 2–3 years’ experience in monitoring pharmaceutical industry clinical trials
Minimum of 1–3 years’ experience monitoring cross therapeutic area clinical trials
Analytical/risk-based monitoring experience is an asset
Ability to actively drive patient recruitment strategies at assigned sites
Ability to partner closely with investigators and site staff to meet study timelines
Ability to operate and use CTMS, EDC, eTMF, dashboards/metrics, IWRS, and safety reporting systems
Strong communication and influencing skills to manage study sites remotely and face to face
Strong team member and self-starter able to work independently
In-depth knowledge of Good Clinical Practice, ICH guidelines, and local regulatory requirements
Legally authorized to work in the United States
Must not require now or in the future sponsorship for employment visa status

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