ICON plc

HQ
Dublin
Total Offices: 29
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

Senior CRA

31 Minutes AgoSaved
In-Office
Shanghai, Shanghai Municipality, Shanghai, CHN
Healthtech • Biotech • Pharmaceutical • Manufacturing
Conduct clinical trial site qualification, initiation, monitoring, and close-out visits. Ensure protocol compliance, data integrity, and patient safety; collaborate with investigators and site staff; review data and resolve queries; and contribute to study documentation, protocols, and clinical study reports. The role is office-based in Shanghai and requires approximately 60% travel.
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ICON plc

Informed Consent Specialist I

31 Minutes AgoSaved
In-Office
3 Locations
Healthtech • Biotech • Pharmaceutical • Manufacturing
Supports the preparation, review, tracking, and management of informed consent documents for clinical research. Responsibilities include coordinating ethics and regulatory approvals, managing templates, translations, and version control, addressing consent-related questions, maintaining audit-ready documentation, and contributing to process improvements. Requires a relevant bachelor’s degree or equivalent experience, basic knowledge of informed consent, GCP, and ethical requirements, strong organizational and communication skills, and proficiency with MS Office and document management systems.
ICON plc Logo
ICON plc

CRA II

31 Minutes AgoSaved
In-Office
Shanghai, Shanghai Municipality, Shanghai, CHN
Healthtech • Biotech • Pharmaceutical • Manufacturing
Conduct clinical trial site qualification, initiation, monitoring, and close-out visits. Ensure protocol compliance, data integrity, and patient safety; collaborate with investigators and site teams; review and resolve data queries; and contribute to protocols and clinical study reports. The role requires approximately 60% travel and is office-based in Shanghai.
see all jobs at ICON plc