Clinical Research Nurse Oncology
at Cone Health
Greensboro, NC 27403, USA -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 25 Nov, 2024 | Not Specified | 30 Aug, 2024 | 1 year(s) or above | Licensure,Red Cross,Ancc | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
OVERVIEW:
The Clinical Research Nurse is responsible for assisting in data collection and analysis specific to clinical research trials. Working under close supervision, the Clinical Research Nurse I supports the research team and occasionally performs some patient-related care and assessments within the scope of their licensure.
Talent Pool: Nursing
EDUCATION:
Required: Associate’s Degree in Nursing
Preferred: Bachelor’s Degree in Nursing
EXPERIENCE:
Required: 1 year as a Registered Nurse
Preferred: 1 year in a clinical specialty as defined by ANCC or national nursing organizations
LICENSURE/CERTIFICATION/REGISTRY/LISTING:Required:
Registered Nurse license in North Carolina or a Compact state
BLS (CPR)-American Red Cross or AHA Healthcare Provide
Responsibilities:
Reviews patient cases, medical histories, and current treatment plans to effectively recruit and enroll potential research subjects that are actively engaged in the informed consent process.
Supports the regulatory process in the submission of study protocols, consent forms, and recruiting materials to the Institutional Review Board and the department for approval, facilitating the regulatory compliance necessary for research projects in the hospital/medical group setting.
Serves as study coordinator for pharmaceutical and/or device trials, successfully coordinating site initiation visits, monitoring visits, and close-out visits, and ensuring adherence to protocol guidelines and regulatory requirements.
Helps coordinate activities for multiple simultaneous clinical trials, managing various research tasks efficiently, ensuring optimal use of resources and executing research protocols in a timely manner.
Corresponds with healthcare teams, providers, outside research partners, and patients, ensuring clear communication and continuity of care for patients.
Assists with the maintenance of records of patient interactions and clinical research interventions to ensure consistent and coordinated care, including collaborating with Investigator in assessment and management of Adverse Events.
Completes clinical tasks within the scope of nursing license to meet patients’ immediate needs as necessary.
Performs other duties as assigned.
REQUIREMENT SUMMARY
Min:1.0Max:6.0 year(s)
Hospital/Health Care
Pharma / Biotech / Healthcare / Medical / R&D
Health Care
Graduate
Nursing
Proficient
1
Greensboro, NC 27403, USA