About The Position

The Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting and assisting in clinical research studies under the supervision of the Principal Investigator or senior clinical research staff. This individual obtains informed consent, collects, maintains and organizes study information. Assists in the preparation and submission of grant applications and documents (e.g., Institutional Review Board, Grants and Contracts Office). The primary goal of this research project is to study the cognitive health of older Chinese Americans. Participants will undergo a standard dementia evaluation that includes a medical exam, cognitive testing, clinical assessment, and a research blood draw.

Requirements

  • Trilingual in Mandarin and Cantonese

Responsibilities

  • Conducting and assisting in clinical research studies
  • Obtaining informed consent
  • Collecting, maintaining, and organizing study information
  • Assisting in the preparation and submission of grant applications and documents (e.g., Institutional Review Board, Grants and Contracts Office)
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