About The Position

The Clinical Research Coordinator I assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information. Assists in preparing grant applications and documents (for e.g., Institutional Review Board, Grants and Contracts Office).

Requirements

  • Industry-Sponsored Clinical Trials Experience

Responsibilities

  • Assists in the daily activities of clinical research studies
  • Obtains informed consent
  • Collects, maintains and organizes study information
  • Assists in preparing grant applications and documents (for e.g., Institutional Review Board, Grants and Contracts Office)
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