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Oversees day-to-day operations of the clinical research site, ensuring compliance, managing staff, and developing budgets to meet objectives.

The Vice President, Sponsor Research Division leads CenExel's sponsor services, overseeing execution, building processes, enhancing partnerships with CROs, and ensuring operational excellence in clinical research.

The Clinical Research Coordinator Sr. coordinates complex clinical trials, manages data compliance, oversees patient involvement, and ensures adherence to protocols and regulations while collaborating with various stakeholders.

The Clinical Research Coordinator II coordinates clinical trials, ensures adherence to regulations, monitors data quality, and educates participants. Responsibilities include administrative tasks, oversight of vendors, and collaborating with the Clinical Trial Manager.

The Clinical Research RN I manages daily clinical study activities, documents research information, recruits participants, and ensures compliance with protocols and safety standards under moderate oversight.

The Clinical Research RN oversees daily clinical study activities, supports participant care, and ensures compliance with research protocols and documentation standards.

Perform clinical and neurocognitive test evaluations on study participants, administer clinical rating scales, and ensure data integrity and adherence to regulations.