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, 842 - Neurosurgery - ISM, Icahn School of Medicine, Neuro Surg
**Responsibilities**
+ 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 ...