Data Coordinator

University of North Carolina at Chapel Hill; Chapel Hill (NC); On-site; USD 56,000 - 65,000; Full time

Job summary

University of North Carolina at Chapel Hill is seeking a Data Coordinator to independently coordinate and manage data entry for oncology treatment trials. The role performs site initiation activities and compiles research patient records in line with federal regulations, Good Clinical Practice, and local policies.

Based in UNC/ACC clinics, the position may include evening/weekend hours and exposure to bloodborne pathogens.

Qualifications

• Hold a bachelor's degree, or an equivalent combination of training and experience.
• Prefer experience with therapeutic clinical research involving drugs or devices.
• Value experience in Phase I, II, and III clinical research.
• Favor experience navigating medical records and extracting data.

Responsibilities

• Enter and manage data for oncology treatment trials.
• Perform site initiation activities for clinical trials.
• Compile research patient records according to federal regulations, Good Clinical Practice, and local policies.
• Work in clinic settings at UNCH or ACC, with occasional evening, weekend, and overtime hours.
• Accept exposure to bloodborne pathogens and hazardous materials.

Skills

Data entry

Data management

Regulatory compliance

Education

Bachelor's degree

Job description

University of North Carolina at Chapel Hill is hiring a Data Coordinator to independently coordinate and manage data entry for oncology treatment trials. The coordinator performs site initiation activities and compiles research patient records according to federal regulations, Good Clinical Practice, and institutional policies. This role supports the UNC / LCCC Protocol Office by protecting research quality, patient safety, and regulatory compliance.

Highlights

• Enter and manage data for oncology treatment trials.
• Perform site initiation activities for clinical trials.
• Compile research patient records according to federal regulations, Good Clinical Practice, and local policies.
• Work in clinic settings at UNCH or ACC, with occasional evening, weekend, and overtime hours.
• Accept exposure to bloodborne pathogens and hazardous materials.
• Hold a bachelor's degree, or an equivalent combination of training and experience.
• Prefer experience with therapeutic clinical research involving drugs or devices.
• Value experience in Phase I, II, and III clinical research.
• Favor experience navigating medical records and extracting data.
• Pay a hiring range of $55,886 to $65,000 per year.