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Oversee daily clinical study activities, provide nursing care, ensure compliance with protocols, conduct informed consent, and maintain study documentation.

The role supports Clinical Research Coordinators by maintaining patient charts, preparing study materials, assisting with assessments, and managing inventory for clinical trials.

Assist in coordinating clinical trials from initiation to completion, ensuring adherence to regulations, organizing data, and reporting findings.

Prepare and manage regulatory documents for clinical research, ensuring compliance with FDA guidelines and training staff accordingly.

The Dietary Aide serves meals to patients, assists with meal preparation, maintains cleanliness in the dining area, and ensures trays are set up according to patient needs.

The Clinical Rater conducts evaluations, interviews, and neurocognitive tests on study participants to assess their psychiatric states per study protocols.

The Research Assistant I supports Clinical Research Coordinators in clinical trials by maintaining patient charts, preparing for participant visits, managing study supplies, and performing data entry and clerical tasks.

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

The Clinical Trial Assistant supports clinical research studies by ensuring compliance, maintaining documentation, and coordinating with research teams and sponsors.

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.