**Job Description**

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).

**Qualifications**

None but a health care background is a plus.

**Responsibilities**

1.Collates and tabulates research data.

2.Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements.

3.Assists in the activities related to clinical research studies including but not limited ...