|Position Type||Permanent Staff (SHRA)|
|Is this an internal only recruitment?||No|
|Position Title||Soc/Clin Research Assistant - Journey|
|Working Title||Regulatory Assistant|
|Budgeted Hiring Range||$40,945 - $45,500|
|Pay Band Information||
To learn more about the pay band for this branch and role, please see the Career Banding rates spreadsheet .
|Salary Grade Equivalent||GN08|
|Full-time/Part-time Permanent/Time-Limited||Full-Time Permanent|
|If time-limited, estimated duration of appointment|
|Hours per week||40|
Monday – Friday; 8:00 a.m. – 5:00 p.m.
|Department Name and Number||LCCC - Clinical Trials-426806|
|Date First Posted||09/01/2020|
|Position Location||Chapel Hill, NC|
|Position Posting Category||Research Professionals|
The UNC Lineberger Comprehensive Cancer Center, founded in 1975, is a National Cancer Institute (NCI)-designated comprehensive cancer center. The Center’s mission is to reduce cancer occurrence and death in North Carolina and the nation through research, treatment, training and outreach.
|Equal Opportunity Employer||
The University of North Carolina at Chapel Hill is an equal opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to age, color, disability, gender, gender expression, gender identity, genetic information, race, national origin, religion, sex, sexual orientation, or status as a protected veteran.
The primary purpose of this position is to provide para-professional support within the Regulatory staff of the Lineberger Protocol Office. The Regulatory Assistant gathers, edits, analyzes, and reports data/information for the purposes of communicating with the Institutional Review Board (IRB) and research sponsors. This work is performed in order to comply with federal, state, and local laws, regulations, and guidances applicable to the conduct of oncology clinical research. Regulatory Assistants participate in the collection, compilation and management of data/information; quality assurance and quality control; analysis by statistical or other means; generation/production of new data/information; and editing and formatting of reports. Regulatory Assistants are expected to use considerable judgment and research skills in performing their work assignments. Work may include the training and supervision of staff, students and others.
|Minimum Education and Experience Requirements||
Bachelor’s degree; or equivalent combination of training and experience. All degrees must be received from appropriately accredited institutions.
|Essential Skills, Knowledge and Abilities||
Working knowledge and facility with information technology; ability to organize, record, and present information; to lead exchange of information through dialog, instruction, and demonstration; ability to develop working knowledge of regulatory compliance and procedures relating to oncology clinical research; ability to communicate professionally both verbally and in writing.
Knowledge of regulatory policy relating to clinical research and institutional review boards.
|Special Physical and Mental Requirements||
Requires sitting for extended periods of time. Ability to move 25 pounds with or without accommodation. Ability and willingness to transport cart with files between 4-5 buildings with or without accommodation.
|Position/Schedule Requirements||Evening work occasionally, Overtime occasionally, Weekend work occasionally|
|Office of Human Resources Contact Information||
If you experience any problems accessing the system or have questions about the application process, please contact the Office of Human Resources at (919) 843-2300 or send an email to firstname.lastname@example.org
Please note: The Office of Human Resources will not be able to provide specific updates regarding position or application status.
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