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Green Life Science · Charlotte, North Carolina
About the Opportunity
An established clinical research site is seeking a motivated and experienced
Clinical Research Nurse (RN)
to join its growing team in Charlotte, NC.
This is an excellent opportunity for a Registered Nurse looking to apply their clinical expertise within a research environment, supporting clinical trial participants and contributing to the delivery of high-quality clinical studies.
The successful candidate will play a key role in participant safety, clinical assessments and protocol-driven research activities, working alongside an experienced team of research professionals.
Key
Conduct participant assessments, obtain vital signs and perform protocol-required clinical procedures.
Support participant screening, enrolment and scheduled clinical trial visits.
Perform phlebotomy, ECGs, specimen collection and processing in accordance with study protocols.
Administer investigational medications and study treatments when authorised and appropriately trained.
Monitor participants for adverse events and changes in clinical status, escalating concerns to the appropriate medical personnel.
Support informed consent procedures in accordance with regulatory requirements and site policies.
Maintain accurate source documentation, nursing notes, medication records and study-related documentation.
Ensure compliance with clinical trial protocols, Good Clinical Practice (GCP), applicable regulations and standard operating procedures.
Collaborate with Principal Investigators, Sub-Investigators, Clinical Research Coordinators and other site staff.
Assist with study preparation, monitoring visits, audits and inspections.
Maintain participant confidentiality and uphold the highest standards of patient safety and ethical research.
Current, active Registered Nurse (RN) licence.
Previous nursing experience in a hospital, outpatient clinic, physician's office or similar patient-facing healthcare environment.
Ability to follow detailed protocols and manage multiple participant visits in a fast-paced environment.
Strong commitment to patient safety, confidentiality and regulatory compliance.
Preferred
Previous experience as a Clinical Research Nurse or within a clinical research site.
Knowledge of ICH-GCP, FDA regulations and clinical research documentation.
Experience with investigational product administration and adverse event reporting.
Familiarity with electronic medical records and clinical trial management systems.
The Opportunity
Work within a collaborative clinical research environment.
Contribute to studies that advance medical knowledge and treatment development.
Develop your clinical research expertise and broaden your experience across clinical trials.
Join a team committed to participant safety and research quality.
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Details
| Company | Green Life Science |
| Location | Charlotte, North Carolina |
| Type | FULL TIME |
| Niche | Health professionals |