Clinical Research Coordinator II-Pediatrics

<br><b>Description</b><p>Under minimal supervision, coordinates the clinical assessments of the study subjects; analyzes and assists in interpreting moderately complex clinical research data. Prepares grant applications and documents and assists in protocol submissions (for e.g., Institutional Review Board, Grants and Contracts Office).</p><br><b>Responsibilities</b><p>1. Analyzes moderately complex clinical research data; Assists in interpreting clinical research data.</p>
<p>2. Coordinates the clinical assessments of the study subjects including but not limited to screening and evaluation of the study subjects.</p>
<p>3. Prepares and ensures grant applications, IRB/GCO documents are submitted.</p>
<p>4. Ensures accurate and complete compilation of subject data through chart reviews.</p>
<p>5. Assists the Principal Investigator and regulatory staff in the preparation of new protocol submissions, protocol amendments, and renewals of ongoing clinical trials.</p>
<p>6. 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.</p>
<p>7. Independently obtains informed consent for other clinical studies.</p>
<p>8. Mentors Clinical Research Coordinators in training.</p>
<p>9. Performs other related duties.</p><br><b>Qualifications</b><ul>
<li>Bachelors degree in sciences or related field.</li>
<li>2 years of clinical research</li>
</ul><br><b>Employer Description</b><p class=