Jobs at Fortrea

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.

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.

Monitors Phase I clinical trial sites, conducts site initiation and close-out visits, verifies informed consent and protocol compliance, reviews clinical data and resolves queries, manages study files and registries, reports serious adverse events, supports project coordination, and trains new employees. The role requires frequent overnight travel and adherence to strict clinical research standards.

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.

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.

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.

Conduct clinical trial site monitoring for ophthalmology studies, including site initiation, routine monitoring, close-out visits, site management, registry management, CRF review, data queries, and serious adverse event reporting. Ensure informed consent, protocol compliance, patient safety, and data integrity. Coordinate with vendors and study teams, support employee training, and manage frequent regional and occasional domestic or international travel.

Lead on-site clinical monitoring and site management for oncology studies, ensuring protocol compliance, informed consent, data integrity (CRF review/query resolution), SAE reporting, registry management, initiation and close-out visits, vendor liaison, training/co-monitoring, and acting as local project coordinator. Significant travel to study sites required.

Lead and conduct on-site clinical trial monitoring for radiopharmaceutical therapy studies, ensuring protocol adherence, patient safety, informed consent, CRF/data integrity, SAE reporting, site management, feasibility, and training. Act as local project coordinator and client contact as assigned, perform monitoring visits, close-outs, and data query resolution using sponsor/CRO data systems.

Lead and perform on-site clinical monitoring for oncology CAR-T trials including site initiation, routine and close-out visits, CRF review, SAE reporting, source document verification, vendor liaison, feasibility, registry management, and training/co-monitoring responsibilities.