ICON plc

Brentwood
Total Offices: 23
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

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ICON plc

Clinical Research Associate II

2 Days AgoSaved
In-Office or Remote
6 Locations
Healthtech • Biotech • Pharmaceutical • Manufacturing
Conduct site selection, initiation, monitoring, and close-out visits across clinical trials. Ensure compliance with ICH-GCP, regulations, and SOPs; maintain CTMS and eTMF documentation; monitor patient safety, drug accountability, recruitment, retention, and data quality; resolve site issues; track training, budgets, and payments; and collaborate with clinical teams.
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ICON plc

Senior Clinical Research Associate

2 Days AgoSaved
In-Office or Remote
7 Locations
Healthtech • Biotech • Pharmaceutical • Manufacturing
Conduct site selection, initiation, monitoring, and close-out visits for clinical research studies. Serve as the sponsor-site contact, ensure ICH-GCP and regulatory compliance, maintain CTMS and eTMF documentation, monitor patient safety and drug accountability, support recruitment and retention, resolve data queries, track site progress and payments, and escalate risks while collaborating with clinical trial partners.
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ICON plc

CRA

2 Days AgoSaved
In-Office or Remote
7 Locations
Healthtech • Biotech • Pharmaceutical • Manufacturing
Conduct clinical trial monitoring for early-stage oncology studies, including site qualification, initiation, monitoring, and close-out visits. Ensure protocol compliance, data integrity, and patient safety; collaborate with investigators and site staff; resolve data queries; and support clinical study documentation. Requires at least two years of Clinical Research Associate experience, oncology monitoring expertise, a scientific or healthcare degree, and willingness to travel up to 50% within the assigned region.
see all jobs at ICON plc