Clinical Research Coordinator

<strong>Clinical Research Coordinator Voted &ldquo;America's Best Hospitals&rdquo; by U.S. News &amp; World.<br /></strong>At Medix, we are passionate about positively impacting your job search by thoroughly understanding your skills, aptitudes and aspirations while ensuring you are matched to an environment and opportunity that fits your goals.&nbsp;<span class="s1">As a national organization, Medix places talent coast-to-coast within the Healthcare, Scientific and Information Technology industries.</span>

Various US Cities (see overview for details)

Medix - Clinical Research

<p><strong>Clinical Research Professionals: Thank you for choosing to build your career in Research!&nbsp;</strong>With less than 2% unemployment in your field and a huge increase in clinical trials, your skills are in high demand!&nbsp;At Medix, we are passionate about positively impacting your job search by thoroughly understanding your skills, aptitudes, and aspirations while ensuring you are matched to an environment and opportunity that fits your goals. As a national organization, Medix places talent coast-to-coast within the Healthcare, Scientific and Information Technology industries.</p> <p><strong>&nbsp;</strong>Check us out on Social Media for the latest and greatest Clinical Research Opportunities. Please feel free to reach out directly OR 480-308-2175</p> http://www.medixteam.com/clinical-research/

keywords: research,openings,contact,research,recruiting,accounting,license,degree,experience

Experienced

Overview: <p>Under the director of the Medical Office Administrator, the Clinical Research Coordinator has working knowledge of clinical research activities and is responsible for the coordination of clinical research protocols, working under compliance with federal regulations, good clinical practice (GCP), Institutional Review Board (IRB) guidelines, department standard work, and performance within their scope of practice.&nbsp;</p> <p>Please feel free to reach out directly: OR 480-308-2175</p> <strong><br />Current openings in the following cities</strong><br /> <ul> <li>Los Angeles, CA</li> <li>Orange County, CA</li> <li>Dallas, TX</li> <li>Phoenix &amp; Tucson, AZ</li> <li>Baltimore, MD</li> <li>Seattle, WA</li> <li>Houston, TX</li> <li>Kansas City, MO</li> </ul> <br />
Responsibilities: <ul> <li>Coordinates research activities in consultation with the Investigator, Research Program</li> <li>Manager, protocol, and sponsor in a safe, efficient and cost-effective manner.</li> <li>Performs data collection procedures as directed by the research protocol with accurate, thorough source documentation and submits data sponsor in a timely manner.</li> <li>Works with PI and Research Program Manager for input to ultimately submit to local or central IRB.&nbsp;</li> </ul>
Requirements: <ul> <li>Bachelor's Degree &nbsp;</li> <li>Oncology Experience</li> <li>Hematology Experience</li> <li>Multi-Therapeutic Experience&nbsp;</li> <li>MUST HAVE 2+ years Clinical Research Experience</li> </ul>