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Clinical Research Data Coordinator

Job in Chapel Hill, Orange County, North Carolina, 27517, USA
Listing for: UNC
Full Time position
Listed on 2026-01-17
Job specializations:
  • Research/Development
    Clinical Research, Data Scientist
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

This position will serve as a Clinical Research Data Coordinator to Dr. Chemtai Mungo in the Department of Obstetrics and Gynecology, Division of Global Women's Health, at UNC Chapel Hill. Dr. Mungo is an OB‑ enfer physician researcher who is passionate about pursuing equity in global women's health. Dr. Mungo's karma research is focused on building evidence for self‑administered therapies for cervical precancer treatment in low‑ and middle‑income countries through clinical trials.

The deskundige is responsible for research data management for a variety of complex clinical research protocols, including leading efforts in compiling, verifying, managing, and reporting data. The coordinate also conducts various quality assurance and quality control efforts to ensure the accuracy of research data. The coordinator is expected to use considerable judgement and research skills to carry out data‑based research tasks.

This position will be responsible for managing research data for a variety of clinical protocols, including compiling, verifying, managing, cleaning, and auditing data, and overseeing quality assurance and quality control activities. The role includes organizing and maintaining data systems for qualitative and quantitative studies, conducting preliminary analyses, and developing reports, metrics, and visualizations to inform study progress, manuscripts, and grant applications.

The coordinator will also contribute to project planning and implementation by collaborating with team members to track study progress and proactively address barriers. The role will support grant writing and dissemination activities by assisting with literature reviews, manuscript drafting, and editing. The position requires strong organizational skills, independent problem‑solving, and the ability to collaborate across teams to ensure accurate data management and timely delivery of research outputs.

Responsibilities
  • Manage research data for a variety of clinical protocols, including compiling, verifying, managing, cleaning, and auditing data, and overseeing quality assurance and quality control activities.
  • Organize and maintain data systems for qualitative and quantitative studies, conduct preliminary analyses, and develop reports, metrics, and visualizations to inform study progress, manuscripts, and grant applications.
  • Coordinate project planning and implementation with team members to track study progress and proactively address barriers.
  • Support grant writing and dissemination activities by assisting with literature reviews, manuscript drafting, and editing.
  • Ensure strong organizational skills, independent problem‑solving, and collaboration across teams to maintain accurate data management and timely delivery of research outputs.
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