Clinical Research Coordinator, Part-Time-Department of Psychiatry
Mount Sinai Health System
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- Location
- United States
- Job type
- Part time
- Posted
- Oct 2
- 18 days ago
Career path
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About the company
Mount Sinai Health System
Hospital & health care · 10,001+ employees
What you'll do
- Collect and record study data, obtain informed consent, screen and educate participants, and assist with research study activities and grant submissions.
- Maintain study files, secure and ship clinical specimens, and prepare for monitoring visits.
What you need
- Bachelors degree in science or related field preferred or a combination of relevant research experience and education.
- Education: a bachelor's degree
Key skills
Informed consentClinical researchStudy dataDatabaseLifestyle questionnairesChart reviewsInstitutional Review Board
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Read the full posting here
The Clinical Research Coordinator, Part-time performs all the regular duties of a Clinical Research Coordinator, but due to abbreviated hours doesn't qualify for exemption. This is an hourly position which is eligible for overtime only intended to be used for part-time employees. The Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information. Assists in preparing grant applications and documents (for e.g., Institutional Review Board, Grants and Contracts Office).
Bachelors degree in science or related field preferred or a combination of relevant research experience and education.
1. Collects and records study data. Inputs all information into database.
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 to: answering phone calls, screening participants for eligibility, registering subjects with sponsoring agency, administering lifestyle questionnaires.
4. Assists in preparing grant applications, IRB/GCO for submission and filings.
5. Maintains source documents and subject files in accordance with hospital procedures. Ensures accurate and complete compilation of subject data through chart reviews.
6. Secures, delivers and ships clinical specimens as required by the protocol.
7. Prepares for monitoring visits.
8. Performs other related duties.