Per Diem Clinical Research Coordinator - Tisch Cancer Center
About The Position
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. 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
Nice To Haves
- 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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What This Job Offers
Job Type
Part-time
Career Level
Entry Level
Number of Employees
5,001-10,000 employees
