Clinical Research Nurse
On-siteStatesville, North Carolina, United States
Job Summary
Perform clinical functions including phlebotomy, vital sign monitoring, and administering study interventions while educating families and determining preliminary inclusion/exclusion criteria. Manage concurrent trials by screening, recruiting, and enrolling participants, coordinating study visits, collecting history, and resolving data queries. Conduct health assessments to monitor adverse events, report safety concerns to investigators, and observe changes in participant status. Collect and ship laboratory specimens, prepare IRB submissions, and maintain compliance with regulatory requirements and SOPs. Provide training to new staff, audit training records, and assist in the informed consent process. Respond to emergencies and provide medical care as directed by the principal investigator.
Required Qualifications
- Current RN/LPN licensure in the state of employment
- Associate Degree in Nursing from an accredited school of nursing
- Certification in Clinical Research Coordination (CCRC) preferred
- BLS required
- Three years prior experience in a health-related clinic or research setting
- Proficient in the use of Microsoft Office applications
- Understanding of medical terminology
- Strong organizational skills
- Working knowledge of clinical trials
- Effective time management skills with the ability to multi-task and manage competing priorities with exceptional attention to detail
- Ability to establish and maintain effective working relationships with physicians, coworkers, managers, and clients
- Practice a high level of integrity, honesty, and in maintaining confidentiality
- Applicants must be authorized to work for ANY employer in the U.S.
- Occasional evening and weekend work may be required as job duties demand
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