Casual RN - Clinical Research & IP Handling

Centricity Research

Morehead City (NC)

Vor Ort

USD 55.000 - 75.000

Teilzeit

Vor 7 Tagen
Sei unter den ersten Bewerbenden

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Benefits dieser Stelle

Health, dental, and vision insurance
Enhanced EAP – mental health support
Flexible PTO + paid holidays
Continuing education reimbursement
401(k) / RRSP with company match and 0

Zusammenfassung

Centricity Research in Morehead City, NC is seeking Registered Nurses to support our team on a casual, as-needed basis at our Morehead City locations. You will provide clinical support for ongoing studies, with emphasis on safe preparation, handling, and administration of investigational products (IP).

You’ll collaborate with Investigators and the clinical research team to ensure study activities comply with protocol, GCP, SOPs, and local regulations while delivering high-quality patient care in

Qualifikationen

  • Active RN license in North Carolina and in good standing.
  • Proficient in medication preparation and injections.
  • Strong phlebotomy, IV placement, and clinical skills.
  • Experience in acute care or clinical research is a plus.

Aufgaben

  • Support ongoing studies with clinical care.
  • Prepare and handle investigational products safely.
  • Perform nursing procedures including phlebotomy, IV placement, injections.
  • Dispense IP and manage inventory per protocol.
  • Document source data, CRFs, and CTMS updates accurately.
  • Maintain Investigator Site Files and study documentation.

Kenntnisse

RN licensure
Intramuscular injections
Phlebotomy
IV placement
Clinical research experience
Patient safety

Ausbildung

Registered Nurse license in North Carolina

Jobbeschreibung

Centricity Research in Morehead City, NC is seeking Registered Nurses to support our team on a casual, as-needed basis at our Morehead City locations. You will provide clinical support for ongoing studies, with emphasis on safe preparation, handling, and administration of investigational products (IP).

You’ll collaborate with Investigators and the clinical research team to ensure study activities comply with protocol, GCP, SOPs, and local regulations while delivering high-quality patient care in

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