ICON plc

Brentwood
Total Offices: 23
34,685 Total Employees
Year Founded: 1990

ICON plc Benefits Overview

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

YesterdaySaved
In-Office
2 Locations
Healthtech • Biotech • Pharmaceutical • Manufacturing
Lead sponsor-side clinical study oversight, managing CROs and vendors (e.g., biometrics, IXRS, eTMF, central labs). Ensure protocol adherence, timelines, budgets, monitoring report review, eTMF/TMF compliance, site readiness, invoice approvals, risk management, audits/inspections, registry updates, and mentor junior team members.
4 Days AgoSaved
In-Office
Cambridge, MA, USA
Healthtech • Biotech • Pharmaceutical • Manufacturing
Lead and perform clinical trial monitoring for Phase I oncology studies, ensuring GCP and protocol compliance. Conduct site visits, manage multiple sites, provide training and guidance to site staff and junior CRAs, collaborate with cross-functional teams, and maintain stakeholder relationships. Frequent travel (~60%) required.
4 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%).