The University of North Carolina at Chapel Hill
Associate Clinical Research Coordinator
The University of North Carolina at Chapel Hill, Raleigh, North Carolina, United States
Position Summary
This position will serve as a temporary Associate Clinical Research Coordinator within the Department of Orthopaedics. The Associate Clinical Research Coordinator is responsible for the execution of clinical research protocols, including leading efforts in participant recruitment, screening, enrollment, and follow‑up visits. Duties also include collecting, entering, and maintaining accurate study data in electronic data capture systems and study databases, serving as a liaison between investigators, study sponsors, clinical staff, and research participants, and performing other research‑related duties as assigned to support continuity of operations. Responsibilities
Execute clinical research protocols, including leading participant recruitment, screening, enrollment, and follow‑up visits. Collect, enter, and maintain accurate study data in electronic data capture systems and study databases. Serve as liaison between investigators, study sponsors, clinical staff, and research participants. Perform other research‑related duties as assigned to support continuity of operations. Qualifications
Demonstrated possession of the competencies necessary to perform the work. Prior experience in collecting research data. Preferred Qualifications
Experience with UNC systems. Equal Opportunity Employer Statement
The University is an equal opportunity employer and welcomes all to apply without regard to age, color, gender, gender expression, gender identity, genetic information, national origin, race, religion, sex, or sexual orientation. We encourage all qualified applicants to apply, including protected veterans and individuals with disabilities.
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This position will serve as a temporary Associate Clinical Research Coordinator within the Department of Orthopaedics. The Associate Clinical Research Coordinator is responsible for the execution of clinical research protocols, including leading efforts in participant recruitment, screening, enrollment, and follow‑up visits. Duties also include collecting, entering, and maintaining accurate study data in electronic data capture systems and study databases, serving as a liaison between investigators, study sponsors, clinical staff, and research participants, and performing other research‑related duties as assigned to support continuity of operations. Responsibilities
Execute clinical research protocols, including leading participant recruitment, screening, enrollment, and follow‑up visits. Collect, enter, and maintain accurate study data in electronic data capture systems and study databases. Serve as liaison between investigators, study sponsors, clinical staff, and research participants. Perform other research‑related duties as assigned to support continuity of operations. Qualifications
Demonstrated possession of the competencies necessary to perform the work. Prior experience in collecting research data. Preferred Qualifications
Experience with UNC systems. Equal Opportunity Employer Statement
The University is an equal opportunity employer and welcomes all to apply without regard to age, color, gender, gender expression, gender identity, genetic information, national origin, race, religion, sex, or sexual orientation. We encourage all qualified applicants to apply, including protected veterans and individuals with disabilities.
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