ICON plc

North Wales
34,685 Total Employees
Year Founded: 1990
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ICON plc Benefits Overview

Compensation + BenefitsWork-Life Balance + WellbeingCareer Growth + DevelopmentCompany Culture

Compensation + Benefits

Offers 401(K)

Offers life insurance

Offers supplemental life insurance

Offers accidental death & dismemberment insurance

Offers disability insurance

Provides a pension

Offers occupational accident insurance

Provides adoption assistance

Provides family medical leave

Offers childcare benefits

Offers generous parental leave

Offers dental insurance

Offers health insurance

Offers mental health benefits

Offers dependent care

Offers Flexible Spending Account (FSA)

Offers vision insurance

Offers Health Savings Account (HSA)

Offers performance bonuses

Offers employee discounts

Work-Life Balance + Wellbeing

Offers company-sponsored outings

Offers gym membership

Offers an Employee Assistance Program (EAP)

Offers generous PTO

Provides paid sick days

Offers unpaid extended leave

Provides paid holidays

Provides bereavement leave

Career Growth + Development

Provides customized development tracks

Job training & conferences

Provides tuition assistance

Company Culture

Utilizes a flexible work schedule

Offers a remote work program

Offers diversity-based Employee Resource Groups

Recently posted jobs

See all jobs at ICON plc
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ICON plc

Clinical Research Associate II

8 Days AgoSaved
In-Office
5 Locations
Healthtech • Biotech • Pharmaceutical • Manufacturing
Serve as primary contact between investigational sites and sponsor to conduct site selection, initiation, routine monitoring, and close-out. Ensure ICH-GCP and regulatory compliance, maintain CTMS/eTMF documentation, monitor patient safety (AE/SAE/PQC), support recruitment and drug accountability, resolve data queries, track site training and budgets, escalate risks, and collaborate with cross-functional clinical teams.
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ICON plc

Senior Clinical Research Associate

8 Days AgoSaved
In-Office
5 Locations
Healthtech • Biotech • Pharmaceutical • Manufacturing
Lead on-site clinical monitoring for oncology/hematology trials: conduct site selection, initiation, routine and close-out visits; ensure ICH-GCP and regulatory compliance; maintain CTMS/eTMF documentation; monitor patient safety and AE/SAE reporting; oversee drug accountability, support recruitment and retention, resolve data queries, track site budgets, and escalate risks to clinical teams while collaborating cross-functionally.
ICON plc Logo
ICON plc

Senior Clinical Research Associate

2 Days AgoSaved
In-Office or Remote
4 Locations
Healthtech • Biotech • Pharmaceutical • Manufacturing
Lead and perform clinical trial monitoring to ensure protocol, regulatory, and GCP compliance. Conduct site visits, assess performance, resolve issues, support data integrity, collaborate with cross-functional teams, train and mentor site staff and other CRAs, and maintain stakeholder relationships to drive successful trial execution. Focused on oncology and other therapeutic areas on the West Coast.
see all jobs at ICON plc