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).
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.
Obtains informed consent under supervision of the Principal Investigator Clinical Research Manager or Senior Clinical Research Coordinator for studies enrolling vulnerable subjects and for studies involving genetic tests.
Independently obtains informed consent for other clinical studies.
Prepares for monitoring visits.
Performs other related duties.
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 the role is $58661.00 - $73530.00 Annually. 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 AWG - II Vascular Surgery - WST Mount Sinai West
Required Experience:
IC
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