Clinical Research Coordinator manages all aspects of the clinical research studies, oversees the running of several clinical trials, manages the day to day operations of the clinic, coordinators and subjects, as well as interfacing with the Sponsor and the PI.

• Develops, coordinates, and reviews research study procedures to ensure receipt, completeness, and accuracy of research data required for studies.
• Directs conduct of research studies to ensure adherence to protocol and provides updates to PI and management team as needed.
• Coordinates all regulatory aspects, such as preparing regulatory packets, safety reports, adverse events.
• Develops procedures to determine subject eligibility; screens, recruits, and enrolls subjects, ensuring and documenting or all aspects of such.
• Coordinates collection of all trial data and completes Case Report Forms
• Prepares IRB submission documents and informs IRB of amendments to research studies; SAEs, or Unanticipated Problems as needed.
• Oversees drug accountability and maintains drug accountability.
• Maintains research office functionality and requirements for study equipment calibration.
• Recognizes and repairs areas of deficiency
• Game plan study conduct and recruitment of subjects.
• Assist in identifying talent.
• Scheduling of staff, including investigators and research assistants.