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

<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>

keywords: clinical trials,analysis,openings,research,process management,management,maintain,recruiting,leadership,scheduling,analysis,patient care,communication,budget,management,experience,license


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>San Francisco, CA</li> </ul>
Responsibilities: <ul> <li>Primary responsibilities include performing nursing assessments and procedures</li> <li>Participating in the review and preparation of protocols for clinical trials</li> <li>Recruiting and enrolling study subjects, and coordinating visits</li> <li>Obtaining informed consent</li> <li>Scheduling patient admissions related to study procedures</li> <li>Serving as a patient advocate, and educating and counseling patients and families</li> <li>Ensuring that clinical trials are followed by clinical research staff</li> <li>Monitoring patient care, and assessing patient status and treatment side effects</li> <li>Maintaining regulatory documentation and managing IRB submissions and follow-ups and overseeing data collection and management in accordance with trial&nbsp;protocol.</li> <li>Assisting with budget preparation and tracking of expenditures. Performs other duties as assigned.</li> <li>Provide research interventions to clinical research patients.</li> <li>Coordinate daily clinic trial activities and function as a Lead for studies.</li> <li>Facilities onboarding and orientation for new staff.</li> <li>Work closely with Clinical Trials Manager, Principal Investigator, Sponsors, Department Staff, and Physicians.</li> <li>Maintain knowledge and act as Subject Matter Expert for the administration of GCP (Good Clinical Practice) compliance, financials, and research studies.</li> </ul>
Requirements: <ul> <li>Strong multi-tasking, relationship management, computer savvy, time management, and interpersonal skills required.</li> <li>Two (2) years of clinical research experience required.</li> <li>Multi-clinical trials from initiation to completion required.</li> <li>Strong ability to work with minimal supervision.</li> <li>Strong oncology experience required.</li> <li>BSN required.</li> <li>RN license or compact state required.&nbsp;</li> </ul>