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Assist in coordinating clinical trials, ensuring adherence to regulations, organizing research information, and documenting study-related data.

The Principal Investigator conducts and oversees clinical research in psychiatry, ensuring compliance with regulations and quality performance while also supervising research staff and managing study protocols.

The Principal Investigator conducts clinical research, ensures compliance with regulations, manages study staff, and oversees patient safety and data integrity.

Oversee daily operations and administrative functions of clinical research sites, ensuring compliance, managing staff, and developing budgets to meet organizational goals.

The QA Coordinator Sr ensures data quality and participant safety, assists in audits, develops quality assurance programs, and provides training on regulations.

Oversee daily clinical study activities, monitor patient care, document research processes, and communicate with sponsors. Involves recruitment, clinical tasks, and adherence to protocols.

The Quality Assurance Coordinator ensures data quality, participant safety, and adherence to protocols. Responsibilities include audit management, vendor oversight, and training compliance.

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.

The Research Assistant I supports Clinical Research Coordinators by managing patient charts, preparing visits, completing data entry, conducting assessments, and assisting with various clerical tasks in a clinical trial setting.