Clinical Research Nurse

<p><strong>World Leading Research Centers Now Hiring Registered Nurses.</strong> <br />At Medix we are extremely dedicated to our candidates, providing them with the best advice, support and direction during their job search.&nbsp;We work with all of our candidates personally to understand their skills and aspirations and best match them with opportunities that fit their goals. As we place contract, contract-to-hire and direct hire employment plans, we offer the flexibility to accommodate your schedule and needs.&nbsp;</p>

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>

keywords: implementation,analysis,current openings,reporting,relationships,medical,teamwork,compliance,assessment,license,organization,degree,experience,passion


Overview: The position is responsible for the coordination and implementation of clinical trials. This includes protocol analysis, creation of source documents, some data entry, patient care, and follow-up.<br /><br /><strong>Current openings in the following cities:</strong> <ul> <li>Los Angeles, CA</li> <li>Baltimore, MD</li> <li>Dallas &amp; Houston, TX</li> <li>Phoenix, AZ</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>Coordinates the calendar of events for patients on clinical trial protocols, including consent, screening, treatment, and follow up visits</li> <li>Provide nursing care to patients on clinical trial protocols</li> <li>Interviews patients and documents adverse events, concomitant medications, and other protocol specific assessments within 24 hours of patient visit</li> <li>Reviews patient medical history and screening requirements for eligibility using a protocol checklist</li> <li>Provides updates on patient status to investigators, colleagues, and protocol sponsors</li> <li>Participates in team meetings as required to conduct research studies; ensuring protocol compliance and financial sustainability of the program (includes site initiation visits, preparation, and training meetings)</li> <li>Reports all serious adverse events to the sponsor <span data-term="goog_1290040234">within 24 hours</span>of knowledge of the event and provides follow up information as it becomes available</li> <li>Establishes and maintains relationships with patients, hospital personnel, and sponsors while assuring confidentiality of patient information in accordance with HIPAA</li> <li>Creates tools such as checklists, cheat sheets, calendars, and flow sheets to assure protocol compliance, accurate billing, and Good Clinical Practice Guidelines are followed</li> <li>Assists in case report form completion, audit preparation and protocol data locks</li> </ul>
Requirements: <ul> <li>Competent physical assessment skills</li> <li>Adherence to Good Clinical Practice (GCP)</li> <li>Attention to details</li> <li>Ability to multi-task</li> <li>Bachelor's Degree</li> <li>Three or more years as a clinical research coordinator</li> <li>Nursing License</li> <li>Passion for patient care</li> </ul>