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Per Diem Clinical Research Coordinator - Tisch Cancer Center

United States Posted: 2026-01-24 63 Views

Job Overview & Requirements

<br><b>Description</b><p>The Tisch Cancer Center brings together a vast range of renowned specialists and resources for cancer care, and provides access to exceptional medical care for other conditions, as needed.</p><p>&nbsp;</p><p>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).</p><br><b>Responsibilities</b><ul><li>Collates and tabulates research data.&nbsp; &nbsp; &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</li><li>Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements. &nbsp; &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</li><li>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.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</li><li>Assists in preparing grant applications, IRB/GCO for submission and filings.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; &nbsp;</li><li>Maintains source documents and subject files in accordance with hospital procedures. Ensures accurate and complete compilation of subject data through chart reviews.&nbsp;&nbsp; &nbsp;</li><li>May perform phlebotomy functions.&nbsp; &nbsp;</li><li>Secures, delivers and ships clinical specimens as required by the protocol.&nbsp; &nbsp; &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</li><li>Prepares for monitoring visits.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; &nbsp;</li><li>Other assigned duties.</li></ul><br><b>Qualifications</b><ul><li>Bachelor’s in Science or closely related field or equivalent experience</li><li>None but a health care background is a plus</li></ul><br><b>Employer Description</b><p class=
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Job Summary

Category Vacant
Country United States
Employment Type Full Time
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