UTS Oncology Research Vacancies at UNC Chapel Hill

North Carolina State University, United States

Updated: over 1 year ago
Location: Chapel Hill, NORTH CAROLINA
Deadline: ;

Posting Details
Position Information


Posting Number PG192862TM
Position Number 48KS34
Position Type Temporary
Essential Job Duties
The UNC Lineberger Comprehensive Cancer Center is a cancer research and treatment center at the University of North Carolina at Chapel Hill. Serving patients at the N.C. Cancer Hospital, UNC Lineberger is the only public comprehensive cancer center in the state of North Carolina.
One of the leading cancer centers in the nation, UNC Lineberger Comprehensive Cancer Center is located in Chapel Hill, North Carolina. As one of only 52 National Cancer Institute-designated Comprehensive Cancer Centers , UNC Lineberger was rated as exceptional – the highest category – by the National Cancer Institute. The center brings together some of the most exceptional physicians and scientists in the country to investigate and improve the prevention, early detection and treatment of cancer.
With research that spans the spectrum from the laboratory to the bedside to the community, UNC Lineberger faculty work to understand the causes of cancer at the genetic and environmental levels, to conduct groundbreaking laboratory research, and to translate findings into pioneering and innovative clinical trials.
To learn more about Lineberger Comprehensive Cancer Center, please visit the website: https://unclineberger.org/
Employees will be eligible for temporary benefits and perks through NC State University. For more information, please visit: https://onboarding.ncsu.edu/tempperks/
Current openings (please note, these are temporary positions that will be full time hours):
 
The Regulatory Associate ($26.50-$28.00 per hour)  is responsible for regulatory compliance of clinical trials performed by the assigned disease group. The position requires that the person be responsible for IRB submissions and responses and for creating and maintaining professional working relationships with investigators, sponsors, team members, and others.
The Regulatory Assistant ($23.00-$25.00 per hour) is responsible for regulatory compliance of clinical trials performed by the assigned disease group providing para-professional support. The position requires that the person be responsible maintaining regulatory documents including 1572s, Delegation of Authority, and most current versions of all protocol documents. The assistant works with all study team members to provide documents needed for monitoring and auditing of studies.
The Study Coordinator ($26.50-$28.00) is responsible for coordinating multiple complex trials through the protocol life cycles of activation, implementation and closure.  These trials are complex, requiring full knowledge of both GCP and full knowledge of individual research protocols. They will need to independently plan, organize, and evaluate implementation of multiple oncology clinical research projects with knowledge of, and in compliance with, sponsor requirements.  For each trial, they will need to acquire full knowledge of research protocol and related documents, plan and document methodologies for research subject and data management based on this knowledge

The Data Coordinator ($20-25 per hour) is responsible for data entry, review of eligibility, registration of subjects, answering data queries, documentation of deviations, facilitating monitor visits and specimen processing for subjects enrolled to multiple complex therapeutic oncology trials. The chosen individuals will facilitate the conduct of research in compliance with Good Clinical Practice, Federal Regulations, CPO SOPs and individual research protocols.
Is Time Limited No
If Yes, Appointment Length

Department Information


Job City & State Chapel Hill, NC
Department

System Information


Classification Title Temporary-Technical/Paraprofessional
Working Title UTS Oncology Research Vacancies at UNC Chapel Hill

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