Data Coordinator

Job description

Position Type:

Permanent Staff (SHRA)

Is this an internal only recruitment?:


Position Title:

Soc/Clin Research Assistant - Journey

Working Title:

Data Coordinator

Position Number:


Vacancy ID:


Budgeted Hiring Range:

$40,945 - $47,000

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:


Full-time/Part-time Permanent/Time-Limited:

Full-Time Permanent

Hours per week:


Work Schedule:

Mon-Fri; 8:30 a.m. to 5:00 p.m.

Department Name and Number:

LCCC - Clinical Trials-426806

Date First Posted:


Closing Date:


Position Location:

Chapel Hill, NC

Position Posting Category:

Research Professionals

Department Description:

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.

Position Description:

This position will independently coordinate complex clinical research studies and perform site initiation activities, help create data collection forms, and coordinate the comprehensive protocol patient record charts by supervising collection of all inter-departmental data records for assigned studies. Additionally, the position will independently assess patients for eligibility for inclusion in studies. The position will oversee the registration and randomizing of patients into studies and assure accurate data is documented in accordance with clinical research protocols and federal regulations. The position will oversee and/or perform the proper processing and shipping of patient laboratory samples for assigned protocols correctly according to procedures outlined in the protocol/laboratory manual in a timely fashion.

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 of and facility with information technology; ability to organize and analyze information; ability to document procedures and to lead exchange of information through dialogue, instruction, and demonstration; ability to develop working knowledge of proprietary databases sufficient to ensure quality control and quality assurance tasks; ability to manage multiple tasks and projects; ability to develop working knowledge of compliance and procedures relating to oncology clinical research; and ability to communicate professionally both verbally and in writing.

Preferred Qualifications:

Knowledge and experience with data management and clinical research methods.

Position/Schedule Requirements:

Evening work occasionally, Exposure to Bloodborne Pathogens, Exposure to Hazardous Materials, Overtime occasionally

Stimulus/ARRA Funded:





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Job No:
Posted: 3/31/2021
Application Due: 4/14/2021
Work Type: Full Time