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The Sr. CRA 2 is responsible for monitoring clinical trials, ensuring compliance with protocols, managing site activities, and training staff while traveling up to 60%.

The Senior CRA is responsible for site monitoring and management of clinical studies, ensuring adherence to protocols and regulatory guidelines while performing routine and closeout visits, data integrity checks, and managing small projects.

The Project Manager is responsible for overseeing clinical trial activities, managing budgets, negotiating contracts, and ensuring compliance with regulatory requirements at a country level.

Senior Clinical Research Associate responsible for site monitoring, data integrity, SAE reporting, CRF review, site management and feasibility, and coordinating local project activities for oncology studies. Requires heavy travel and training/co-monitoring support duties.

The Senior CRA 2 is responsible for site monitoring, site management, ensuring compliance with regulatory requirements, managing study activities, and leading clinical trials for the company.

As an Oncology CRA II, you'll monitor clinical trials, ensure protocol adherence, manage data integrity, and support site management tasks, while collaborating with teams and vendors.

Lead site monitoring and management for clinical studies, ensuring regulatory compliance, data integrity, SAE tracking, and audit readiness. Conduct initiation, routine, and closeout visits; prepare trip reports; manage small projects, train/mentor junior staff, liaise with vendors, assist protocol/CRF development, and perform local project coordination as assigned. Frequent travel (~50%+), Spanish language ability required.