Clinical Research Coordinator, Part-Time-Emergency Medicine

Mount Sinai Health System

United StatesPart time
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Pay
$17 to $38
an hour
Location
United States
Job type
Part time
Posted
Oct 9
11 days ago
Career path

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About the company

Mount Sinai Health System

Hospital & health care · 10,001+ employees

Mount Sinai Health System on LinkedIn

What you'll do

  • Collects, records, and organizes study data; obtains informed consent and educates participants.
  • Supports study activities, prepares grant and IRB/GCO submissions, maintains study files, handles specimens, and prepares 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

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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. Compensation Statement The Mount Sinai Health System (MSHS) provides salary ranges that comply with the New York City Law on Salary Transparency in Job Advertisements. The salary range for this role is $17.00 - $38.48 Hourly. Actual salaries depend on a variety of factors, including experience, education, and operational need. The salary range or contractual rate listed does not include bonuses/incentive, differential pay or other forms of compensation or benefits. Non-Bargaining Unit, 870 - Emergency Medicine - ISM, Icahn School of Medicine Collects and records study data. Inputs all information into database. 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. Secures, delivers and ships clinical specimens as required by the protocol. Prepares for monitoring visits. Performs other related duties.

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