UNC Health
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Clinical Research Nurse- Endocrinology
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UNC Health 1 day ago Be among the first 25 applicants Join to apply for the
Clinical Research Nurse- Endocrinology
role at
UNC Health Get AI-powered advice on this job and more exclusive features. Description
Become part of an inclusive organization with over 40,000 teammates, whose mission is to improve the health and well-being of the unique communities we serve. Description
Become part of an inclusive organization with over 40,000 teammates, whose mission is to improve the health and well-being of the unique communities we serve.
Summary
The Clinical Research Nurse (RN) is responsible for providing and coordinating clinical care for patients enrolled in a clinical trial while adhering to all FDA, OHRP and GCP guidelines and regulations. This position has a central role in assuring participant safety, ongoing maintenance of informed consent, and integrity of protocol implementation, accuracy of data collection, data recording and follow up.
Responsibilities
Identifies potential clinical trial patients and collaborates with the physician investigator to enroll eligible patients to clinical trials. Serves as a resource to the patient care team for the management of care of patients participating in clinical trials, ensuring compliance with protocol procedures, assessments, reporting requirements, and management of symptoms. Ensures the initial and ongoing consent process is performed and documented in compliance with FDA, International Conference on Harmonization Good Clinical Practice (GCP), institutional, sponsor, IRB, and other applicable regulations and policies. Ensure patient comprehension and safety during initial and ongoing clinical trial informed consent discussions. Counsels and teaches research participants about protocol participation, treatment, and side effects, medication compliance, and administration of investigational drugs. Documents assessment, management, and evaluation in source documents for patients on clinical trials as appropriate to the protocol. Ensures that relevant data from the source document are abstracted and accurately recorded in the clinical trial case report forms and that every data point can be verified within the source document. Organizes charts as required by the sponsor or research group for audits. Collaborates with physician investigators, pharmacy, and other appropriate personnel to ensure proper use of and accountability for investigational drugs. Adheres to protocol guidelines for the collection, processing, and shipping of biospecimens and accurately enters data into the protocol specimen tracker. Complies with the International Air Transport Association and institutional policies for shipping of biological specimens. Ensures that all Research Coordinator responsibilities are completed in EPIC including but not limited to: creating and activating a study record, creating a billing coverage analysis for each study, associating a patient with a research study, linking research encounters to the study, reviewing charges for research patients to ensure Medicare billing compliance, and create treatment plans in Beacon for research patients corresponding to the protocol requirements.
PARDEE
Other Information
Hired applicants will be expected to acquire Society of Clinical Research Associates (SOCRA), Certified Clinical Research Professional (CCRP), Certified Clinical Research Coordinator (CCRC), or Association of Clinical Research Professionals (ACRP) Certified Professional (ACRP-CP).
Required
Must be licensed to practice as a Registered Nurse in the state of North Carolina or one of compact states.
Preferred
Experience managing research pharmaceutical trials in ambulatory setting.
01.8320.1514
Job Details
Legal Employer: Pardee - HCHC
Entity: Pardee UNC Health Care
Organization Unit: Pardee Cancer Research
Work Type: Full Time
Standard Hours Per Week: 40.00
Work Assignment Type: Hybrid
Work Schedule: Day Job
Location of Job: PARDEECANCR
Exempt From Overtime: Exempt: No Seniority level
Seniority level Entry level Employment type
Employment type Full-time Job function
Job function Health Care Provider Industries Wellness and Fitness Services, Hospitals and Health Care, and Medical Practices Referrals increase your chances of interviewing at UNC Health by 2x Get notified about new Clinical Research Nurse jobs in
Hendersonville, NC . Travelers Rest, SC $65,000.00-$75,000.00 1 month ago Asheville, NC $1,986.12-$1,986.12 1 month ago Candler, NC $60,000.00-$90,000.00 6 days ago Marietta, SC $65,000.00-$75,000.00 1 month ago Registered Nurse (RN) - Ambulatory, Primary Care North Greenville, FT, Day
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We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
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Clinical Research Nurse- Endocrinology
role at
UNC Health 1 day ago Be among the first 25 applicants Join to apply for the
Clinical Research Nurse- Endocrinology
role at
UNC Health Get AI-powered advice on this job and more exclusive features. Description
Become part of an inclusive organization with over 40,000 teammates, whose mission is to improve the health and well-being of the unique communities we serve. Description
Become part of an inclusive organization with over 40,000 teammates, whose mission is to improve the health and well-being of the unique communities we serve.
Summary
The Clinical Research Nurse (RN) is responsible for providing and coordinating clinical care for patients enrolled in a clinical trial while adhering to all FDA, OHRP and GCP guidelines and regulations. This position has a central role in assuring participant safety, ongoing maintenance of informed consent, and integrity of protocol implementation, accuracy of data collection, data recording and follow up.
Responsibilities
Identifies potential clinical trial patients and collaborates with the physician investigator to enroll eligible patients to clinical trials. Serves as a resource to the patient care team for the management of care of patients participating in clinical trials, ensuring compliance with protocol procedures, assessments, reporting requirements, and management of symptoms. Ensures the initial and ongoing consent process is performed and documented in compliance with FDA, International Conference on Harmonization Good Clinical Practice (GCP), institutional, sponsor, IRB, and other applicable regulations and policies. Ensure patient comprehension and safety during initial and ongoing clinical trial informed consent discussions. Counsels and teaches research participants about protocol participation, treatment, and side effects, medication compliance, and administration of investigational drugs. Documents assessment, management, and evaluation in source documents for patients on clinical trials as appropriate to the protocol. Ensures that relevant data from the source document are abstracted and accurately recorded in the clinical trial case report forms and that every data point can be verified within the source document. Organizes charts as required by the sponsor or research group for audits. Collaborates with physician investigators, pharmacy, and other appropriate personnel to ensure proper use of and accountability for investigational drugs. Adheres to protocol guidelines for the collection, processing, and shipping of biospecimens and accurately enters data into the protocol specimen tracker. Complies with the International Air Transport Association and institutional policies for shipping of biological specimens. Ensures that all Research Coordinator responsibilities are completed in EPIC including but not limited to: creating and activating a study record, creating a billing coverage analysis for each study, associating a patient with a research study, linking research encounters to the study, reviewing charges for research patients to ensure Medicare billing compliance, and create treatment plans in Beacon for research patients corresponding to the protocol requirements.
PARDEE
Other Information
Hired applicants will be expected to acquire Society of Clinical Research Associates (SOCRA), Certified Clinical Research Professional (CCRP), Certified Clinical Research Coordinator (CCRC), or Association of Clinical Research Professionals (ACRP) Certified Professional (ACRP-CP).
Required
Must be licensed to practice as a Registered Nurse in the state of North Carolina or one of compact states.
Preferred
Experience managing research pharmaceutical trials in ambulatory setting.
01.8320.1514
Job Details
Legal Employer: Pardee - HCHC
Entity: Pardee UNC Health Care
Organization Unit: Pardee Cancer Research
Work Type: Full Time
Standard Hours Per Week: 40.00
Work Assignment Type: Hybrid
Work Schedule: Day Job
Location of Job: PARDEECANCR
Exempt From Overtime: Exempt: No Seniority level
Seniority level Entry level Employment type
Employment type Full-time Job function
Job function Health Care Provider Industries Wellness and Fitness Services, Hospitals and Health Care, and Medical Practices Referrals increase your chances of interviewing at UNC Health by 2x Get notified about new Clinical Research Nurse jobs in
Hendersonville, NC . Travelers Rest, SC $65,000.00-$75,000.00 1 month ago Asheville, NC $1,986.12-$1,986.12 1 month ago Candler, NC $60,000.00-$90,000.00 6 days ago Marietta, SC $65,000.00-$75,000.00 1 month ago Registered Nurse (RN) - Ambulatory, Primary Care North Greenville, FT, Day
Marietta, SC $65,000.00-$75,000.00 1 month ago TRAVEL - RN - ONCOLOGY (632) - Mission Hospital - 7:00AM – 7:00PM
RN / Registered Nurse / Forensic ACTT / $5,000 SIGN ON BONUS
Registered Nurse - Endocrinology Hendersonville
BACKFILL - TRAVEL - RN - PICU (640) - 7:00PM-7:00AM
TRAVEL - RN - INPATIENT REHAB - (693) 7:00PM-7:00AM
Asheville, NC $1,634.47-$1,634.47 1 month ago Candler, NC $60,000.00-$90,000.00 6 days ago Registered Nurse (RN) - Ambulatory, Primary Care North Greenville, FT, Day
Registered Nurse (RN) - Pre-Anesthesia Testing
RN/LPN Full Time **Sign on Bonus** Full time Baylor
Certified Nursing Assistant (CNA) - The Laurels of Hendersonville
Director of Clinical Services (RN) - Carolina Reserve of Hendersonville
Registered Nurse Pediatric Clinical Research
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr