Fortrea
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
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.
Biotech
Conducts clinical trial site monitoring and management, including initiation, routine and close-out visits; verifies informed consent, protocol compliance, patient safety, and data integrity; manages CRFs, queries, serious adverse event reporting, registries, vendors, and study documentation. May train employees and coordinate local clinical projects. Requires 4+ years of clinical monitoring experience, an allied health degree or certification, and more than 50% overnight travel.
Biotech
Conduct clinical trial site monitoring, including pre-study, initiation, routine monitoring, and close-out visits. Ensure protocol compliance, informed consent, participant protection, data integrity, SAE reporting, CRF review, query resolution, registry management, and study file maintenance. Liaise with vendors, support feasibility activities, train new employees, and coordinate designated clinical projects. The role requires frequent domestic and occasional international travel.
