About the Role
<p><strong>THE OPPORTUNITY:</strong></p>
<p>As the Specialist in R&D/Product Development, considered as highly experienced and knowledgeable resource within the organization in overseeing the direction, planning, execution, clinical trials/research and the data collection activities.</p>
<p><strong>Locations: Boston, MA | NYC/Long Island | New England area (NJ, CT, VT, NH, ME)</strong></p>
<p><strong>RESPONSIBILITIES:</strong></p>
<ul>
<li>Contribute to the implementation of clinical protocols and facilitates completion of final reports.</li>
<li>Recruit clinical investigators and negotiate study design and costs.</li>
<li>Responsible for directing human clinical trials, phases III & IV for company products under development.</li>
<li>Participate in adverse event reporting and safety responsibilities monitoring.</li>
<li>Coordinate and provide reporting information for reports submitted to the regulatory agencies.</li>
<li>Monitor adherence to protocols and determine study completion.</li>
<li>Coordinate and oversee investigator initiations and group studies.</li>
<li>May act as a consultant/liaison with other corporations when working under licensing agreements.</li>
</ul>
<p><strong> </strong></p>
<p><strong>EDUCATION and EXPERIENCE:</strong></p>
<p><strong>Required Experience:</strong></p>
<ul>
<li>Associate’s degree required</li>
<li>7 years of Cath Lab and/or Medical Device experience</li>
</ul>
<p><strong>Preferred Experience:</strong></p>
<ul>
<li>Bachelor’s Degree highly preferred.</li>
<li>Coronary and peripheral technologies</li>
<li>Clinical Trial Support experience</li>
<li>Product Development</li>
<li>Cath Lab Tech or Surgical Tech</li>
<li>Medical Device experience</li>
<li>OCT experience</li>
</ul>