Fortrea

HQ
Durham
10,811 Total Employees

Fortrea Benefits Overview

Compensation + Benefits

Offers 401(K)

Offers life insurance

Offers accidental death & dismemberment insurance

Offers disability insurance

Offers occupational accident insurance

Offers childcare benefits

Offers generous parental leave

Offers dental insurance

Offers health insurance

Offers mental health benefits

Offers Flexible Spending Account (FSA)

Offers vision insurance

Offers employee stock purchase plan

Offers performance bonuses

Career Growth + Development

Provides customized development tracks

Job training & conferences

Provides tuition assistance

Offers apprenticeship programs

Work-Life Balance + Wellbeing

Offers generous PTO

Provides paid sick days

Provides paid holidays

Provides bereavement leave

Offers an Employee Assistance Program (EAP)

Company Culture

Offers a remote work program

Offers diversity-based Employee Resource Groups

Recently posted jobs

17 Hours AgoSaved
Remote
2 Locations
Biotech
Oversee clinical trial start-up and delivery from site identification through database lock. Manage timelines, budgets, risks, regulatory and ethics submissions, site selection, contracts, supplies, recruitment, monitoring, quality, documentation, and site payments. Lead client communications and collaborate with global cross-functional teams to ensure compliance, patient safety, data integrity, inspection readiness, and successful trial execution.
2 Days AgoSaved
Remote
United States
Biotech
Coordinates clinical study site start-up and maintenance activities, including collecting and reviewing essential documents, preparing regulatory and IRB/IEC submissions, tracking approvals, updating electronic systems, and ensuring compliance with ICH/GCP, regulations, SOPs, timelines, and quality standards. Acts as a primary contact for investigative sites and regulatory bodies, supports informed consent customization, contract and budget tracking, risk escalation, and site activation strategy. May mentor less-experienced colleagues and requires frequent domestic and international travel.
Biotech
Conducts oncology clinical trial site monitoring, including routine, initiation, and close-out visits; verifies informed consent, protocol compliance, patient safety, and data integrity; manages study files, registries, vendors, and serious adverse event reporting; performs CRF review and query resolution; supports feasibility activities, employee training, and local project coordination. Requires frequent overnight travel across Southern California and occasional domestic or international travel.