Clinical Research Coordinator I-OB/GYN

<br><b>Description</b><p>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).</p><br><b>Responsibilities</b><ul><li>Collects and records study data. Inputs all information into database.</li><li>Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements.</li><li>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.</li><li>Assists in preparing grant applications, IRB/GCO for submission and filings.</li><li>Maintains source documents and subject files in accordance with hospital procedures. Ensures accurate and complete compilation of subject data through chart reviews.</li><li>Secures, delivers and ships clinical specimens as required by the protocol.</li><li>Prepares for monitoring visits.</li><li>Performs other related duties.</li></ul><br><b>Qualifications</b><ul>
<li>Bachelors or Masters degree in Science or closely related field.</li>
<li>No experience required. One year of research experience preferred.</li>
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