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

<h3>Launched in 2001, Medix was built on the principle of becoming a leading provider of workforce solutions for clients and candidates across the Healthcare, Scientific and Information Technology industries.&nbsp;As we grow and evolve, we recognize our differentiation lies not just in traditional staffing, but in true partnerships and collaboration on hiring solutions. We bring value to our talent by helping them identify their individual skills and aptitudes, matching them with opportunities to excel and creating communities where they can foster their skills and always have a trusted partner in their career.&nbsp;In supporting our clients, we understand that each organization and culture is unique, and we thrive in collaborating with our clients to provide innovative solutions to suit their specific needs.</h3> http://www.medixteam.com

keywords: research,reporting,research,recruiting,accounting,license,degree,experience

Experienced

Overview: The candidate will be coordinating clinical research protocols from study start up to close out. This candidate will work closely with all research staff to collect, store and maintain data in accordance with FDA Regulations, International Council of Harmonization and Good Clinical Practices.<br /><strong><br />Current openings in the following cities:</strong> <ul> <li>Los Angeles, CA - Report.</li> <li>Dallas, TX</li> <li>Phoenix &amp; Tucson, AZ</li> <li>Baltimore, MA</li> <li>Seattle, WA</li> <li>Wheaton, MD</li> <li>Hillsborough, NJ</li> <li>Tacoma, WA</li> <li>Fullerton, CA</li> <li></li> </ul>
Responsibilities: <ul> <li>May be the sole coordinator or work in collaboration with a research nurse on studies, responsible for source documents, data collection, data entry, query resolution, triggering financial payments, study close out and liaison with the sponsor/CRO</li> <li>Participates in the identification of potential clinical trial participants, screens them for eligibility, and enrolls participants per protocol</li> <li>Coordinates the schedule of events for clinical trial participants from screening to follow up according to protocol</li> <li>Collects, verifies, organizes and records clinical information and data in electronic data capture systems (EDC). Abstracts data from necessary sources to complete the EDC and resolve queries. Performs the following data related activities: EDC tracking, reviewing validation, updating, SAE reconciliation, lab data reconciliation and safety coding</li> <li>May be responsible for regulatory submissions. Need working knowledge of essential documents and IRB requirements</li> <li>Participates in site feasibility determination, site qualification visits, site initiation visits and research related meetings</li> <li>May be responsible for recruiting clinical trials to site</li> <li>May or may not have patient contact (dependent of set up of site)</li> </ul>
Requirements: <ul> <li>Bachelor's Degree</li> <li>2 years experience</li> <li>May require a RN</li> </ul>