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

See all jobs at ICON plc
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ICON plc

Feasibility Informatics Manager

23 Days AgoSaved
In-Office or Remote
23 Locations
Healthtech • Biotech • Pharmaceutical • Manufacturing
Lead feasibility informatics strategy for clinical trial proposals and awarded feasibility projects. Provide data-driven feasibility analyses using internal/external data, support bid defenses, manage delivery and handover to site identification, assess risks, and collaborate with cross-functional teams to meet sponsor objectives.
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ICON plc

Clinical Study Specialist

27 Days AgoSaved
In-Office
2 Locations
Healthtech • Biotech • Pharmaceutical • Manufacturing
Supports global clinical trials by coordinating study meetings, documents, reports, site activation, enrollment, monitoring, TMF reconciliation, vendor oversight, and study closeout activities. Maintains trial systems, investigator and site information, regulatory materials, clinical trial registry updates, and study communications. Contributes to document reviews, training materials, process improvements, and SOP revisions.
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ICON plc

Senior CRA

29 Days AgoSaved
In-Office
Cambridge, MA, USA
Healthtech • Biotech • Pharmaceutical • Manufacturing
Lead monitoring activities for Phase I oncology clinical trials, ensure GCP/regulatory compliance, conduct site visits, train and guide site staff and other CRAs, manage multiple sites, collaborate with cross-functional teams, and maintain data integrity while traveling to sites (~60%).
see all jobs at ICON plc