Study Coordinator/Nurse Consultant
Full Time
Chapel Hill, NC 27599
Posted
Job description
Posting Information
Department
LCCC - Clinical Trials-426806
Career Area
Research Professionals
Is this an internal only recruitment?
No
Posting Open Date
09/01/2022
Application Deadline
09/15/2022
Position Type
Permanent Staff (SHRA)
Position Title
Nurse Consultant - Journey
Salary Grade Equivalent
GN13
Working Title
Study Coordinator/Nurse Consultant
Position Number
00060237
Vacancy ID
P015996
Full-time/Part-time Permanent/Time-Limited
Full-Time Permanent
If time-limited, estimated duration of appointment
Hours per week
40
Work Schedule
Monday – Friday 8:00AM – 5:00PM
Work Location
Chapel Hill, NC
Position Location
North Carolina, US
Hiring Range
$63,972 - $83,489
Pay Band Information
To learn more about the pay band for this branch and role, please see
the Career Banding rates spreadsheet.
Position Summary Information
Primary Purpose of Organizational Unit
The UNC Lineberger Comprehensive Cancer Center, founded in 1975, is one of 47 National Cancer Institute (NCI)-designated comprehensive cancer centers in the country. The Center’s mission is to reduce cancer occurrence and death in North Carolina and the nation through research, treatment, training and outreach.
The UNC/LCCC Protocol Office is an established clinical facility designed to serve as a core resource for the development and conduct of oncology clinical research for investigators in all disciplines. The Protocol Office staff, are responsible for protecting the safety of patients, ensuring the quality of the research, and safeguarding the interests of the University. The Protocol Office provides administrative, regulatory, data management, and study coordination services to investigators throughout the process of development, approval and implementation of protocols conducted at UNC-CH and its affiliate institutions. The Protocol Office also provides guidance and input focused on clinical research systems development and decision-making and is a liaison with the hospital pharmacy, laboratory, radiology, clinics, public relations, and medical records department for protocol-related activity and information. In addition, the Protocol Office also furnishes protocol-related information to health professionals and to the community at large.
The UNC/LCCC Protocol Office is an established clinical facility designed to serve as a core resource for the development and conduct of oncology clinical research for investigators in all disciplines. The Protocol Office staff, are responsible for protecting the safety of patients, ensuring the quality of the research, and safeguarding the interests of the University. The Protocol Office provides administrative, regulatory, data management, and study coordination services to investigators throughout the process of development, approval and implementation of protocols conducted at UNC-CH and its affiliate institutions. The Protocol Office also provides guidance and input focused on clinical research systems development and decision-making and is a liaison with the hospital pharmacy, laboratory, radiology, clinics, public relations, and medical records department for protocol-related activity and information. In addition, the Protocol Office also furnishes protocol-related information to health professionals and to the community at large.
Position Summary
The purpose of this position is to facilitate the conduct of oncology clinical trials, including subject and data management, according to federal regulations, Good Clinical Practice, and local and institutional policies. These responsibilities relate to the mission of the UNC/LCCC Protocol Office by maintaining the quality of research and by addressing patient safety and regulatory compliance which impact research quality and safeguard institutional integrity.
Minimum Education and Experience Requirements
Licensed to practice as a Registered Nurse in the State of North Carolina and two years of experience in the area of specialization.
Required Qualifications, Competencies, and Experience
Knowledge of ICH GCP, Federal Regulations and Guidelines and ability to follow established regulations, procedures, and protocols; strong computer skills; ability to gather data and document procedures; ability to plan work and coordinate multiple projects; adequate social acumen and customer service skills; ability to communicate effectively and professionally verbally and in writing. Study Coordinator 1 requires one year of study coordinator experience or experience in oncology clinical trials. Study Coordinator 2 requires two years of study coordinator experience and one year of oncology study coordinator experience.
Ability to work on evenings, weekends and/or holidays occasionally required.
Ability to work on evenings, weekends and/or holidays occasionally required.
Preferred Qualifications, Competencies, and Experience
Bachelor’s Degree in a related field.
Previous experience with therapeutic clinical research involving drugs and/or devices.
Experience in Phase I, II, and III clinical research.
Experience navigating medical records and data extraction.
SOCRA/ACRP Certification
Study Coordinator 1, one year of study coordinator experience or experience in oncology clinical trials preferred. Study Coordinator 2, two years of study coordinator experience and one year of oncology study coordinator experience preferred.
Previous experience with therapeutic clinical research involving drugs and/or devices.
Experience in Phase I, II, and III clinical research.
Experience navigating medical records and data extraction.
SOCRA/ACRP Certification
Study Coordinator 1, one year of study coordinator experience or experience in oncology clinical trials preferred. Study Coordinator 2, two years of study coordinator experience and one year of oncology study coordinator experience preferred.
Required Licenses/Certifications
Licensed to practice as a Registered Nurse in the State of North Carolina
Special Physical/Mental Requirements
Campus Security Authority Responsibilities
Not Applicable.
Position/Schedule Requirements
Clinic – UNCH or ACC, Evening work occasionally, Exposure to Bloodborne Pathogens, Exposure to Hazardous Materials, Laboratory, Overtime occasionally, Weekend work occasionally
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