Mount Sinai Health System
Clinical Research Coordinator I-Psychiatry Dr. Li
Mount Sinai Health System, New York, New York, us, 10261
Job Description
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). Responsibilities
Collect and record study data. Obtain informed consent under minimal supervision of the investigator(s) and educate participants regarding study requirements. Assist in activities related to clinical research studies including answering phone calls, screening participants for eligibility, registering subjects with sponsoring agency, administering lifestyle questionnaires. Assist in preparing grant applications, IRB/GCO for submission and filings. Maintain source documents and subject files in accordance with hospital procedures. Ensure accurate and complete compilation of subject data through chart reviews. Secure, deliver and ship clinical specimens as required by the protocol. Prepare for monitoring visits. Perform other related duties. Qualifications
Bachelors or Masters degree in Science or closely related field. 1-2 years of research experience. Equal Opportunity Employer
The Mount Sinai Health System is an equal opportunity employer, complying with all applicable federal civil rights laws. We do not discriminate, exclude, or treat individuals differently based on race, color, national origin, age, religion, disability, sex, sexual orientation, gender, veteran status, or any other characteristic protected by law.
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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). Responsibilities
Collect and record study data. Obtain informed consent under minimal supervision of the investigator(s) and educate participants regarding study requirements. Assist in activities related to clinical research studies including answering phone calls, screening participants for eligibility, registering subjects with sponsoring agency, administering lifestyle questionnaires. Assist in preparing grant applications, IRB/GCO for submission and filings. Maintain source documents and subject files in accordance with hospital procedures. Ensure accurate and complete compilation of subject data through chart reviews. Secure, deliver and ship clinical specimens as required by the protocol. Prepare for monitoring visits. Perform other related duties. Qualifications
Bachelors or Masters degree in Science or closely related field. 1-2 years of research experience. Equal Opportunity Employer
The Mount Sinai Health System is an equal opportunity employer, complying with all applicable federal civil rights laws. We do not discriminate, exclude, or treat individuals differently based on race, color, national origin, age, religion, disability, sex, sexual orientation, gender, veteran status, or any other characteristic protected by law.
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