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

The Assistant Nurse Manager supervises Clinical Research Nurses and Psychiatric Technicians, ensuring compliance and optimal patient care within the Critical Research Unit. They foster teamwork, coordinate staffing, and support staff development and training efforts.

The Research Assistant I supports Clinical Research Coordinators by managing patient charts, data entry, and facilitating study activities, ensuring compliance with protocol guidelines.

The Quality Assurance Coordinator ensures data quality and participant safety in clinical trials, adhering to protocols and regulations while supporting QA programs and audits.

Coordinate all aspects of clinical trials from initiation to completion, ensuring adherence to protocols and regulations while managing patient involvement and data analysis.

The Clinical Research RN I oversees clinical study activities, ensures compliance with protocols, provides nursing care, and maintains documentation. They serve as a liaison between the site and sponsor, conduct assessments, and manage study logistics.

The Research Assistant I supports Clinical Research Coordinators by maintaining patient charts, preparing materials for visits, completing data entry, and assisting participants, while adhering to study protocols and guidelines.

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

The Regulatory Coordinator is responsible for regulatory document preparation, submissions, and coordination with sponsors and IRBs while maintaining compliance with FDA guidelines and GCP.

The PRN-Clinical Research RN I oversees clinical study activities, providing nursing care to participants, documenting studies, and ensuring compliance with protocols.