About The Position

The Per Diem Clinical Research Coordinator performs all the regular duties of a full or part time Clinical Research Coordinator, but on an as-needed basis. In addition, due to a limited number of hours, does not apply for Exempt status as is normal in this group. This individual assists in activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information, and may perform phlebotomy duties. Assists in preparing grant applications and documents (for e.g., Institutional Review Board, Grants and Contracts Office).

Requirements

  • Bachelor’s in Science or closely related field or equivalent experience
  • None but a health care background is a plus.

Responsibilities

  • Collates and tabulates research data.
  • Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements.
  • Assists in the activities related to clinical research studies including but not limited to: answering phone calls, screening participants for eligibility, registering subjects with sponsoring agency, administering lifestyle questionnaires.
  • Assists in preparing grant applications, IRB/GCO for submission and filings.
  • Maintains source documents and subject files in accordance with hospital procedures.
  • Ensures accurate and complete compilation of subject data through chart reviews.
  • May perform phlebotomy functions.
  • Secures, delivers and ships clinical specimens as required by the protocol.
  • Prepares for monitoring visits.
  • Other assigned duties.
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