Opportunity Description
**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).
**Qualifications**
+ Bachelors or Masters degree in Science or closely related field.
+ No experience required. One year of research experience preferred.
Non-Bargaining Unit, 845 - Orthopaedics - ISM, Icahn School of Medicine
**Responsibilities**
+ 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, register...
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).
**Qualifications**
+ Bachelors or Masters degree in Science or closely related field.
+ No experience required. One year of research experience preferred.
Non-Bargaining Unit, 845 - Orthopaedics - ISM, Icahn School of Medicine
**Responsibilities**
+ 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, register...
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