Associate Clinical Research Coordinator
About The Position
The primary purpose of this position is to serve as an Associate Clinical Research Coordinator of clinical research projects in melanoma. The Associate Clinical Research Coordinator is responsible for the execution of clinical research protocols, including leading the efforts in gathering, compiling, and reporting data for a variety of research studies. The position will be responsible for the organization and management of the UNC Melanoma and Complex Skin Cancer Registry and other cancer study databases. The responsibilities include identification and recruitment of eligible populations, collection and compilation of data, and conveying accurate information to clinical investigators, basic scientists, bioinformaticians, and the UNC Institutional Review Board and/or Clinical Protocol Office while adhering to CITI research ethics and HIPAA regulations. This position will establish an overall plan for the administration of ongoing research projects and will serve as the contact person for the study participants, research personnel, work study students, and investigators. The selected candidate will be responsible for maintaining relationship and encouraging collaborate research with multiple clinicians and researchers. The position will also assist in preparation of manuscripts and presentations.
Requirements
- Adherence to CITI research ethics and HIPAA regulations.
Responsibilities
- Serve as an Associate Clinical Research Coordinator of clinical research projects in melanoma.
- Execute clinical research protocols, including gathering, compiling, and reporting data for research studies.
- Organize and manage the UNC Melanoma and Complex Skin Cancer Registry and other cancer study databases.
- Identify and recruit eligible populations for studies.
- Collect and compile data.
- Convey accurate information to clinical investigators, basic scientists, bioinformaticians, and the UNC Institutional Review Board and/or Clinical Protocol Office while adhering to CITI research ethics and HIPAA regulations.
- Establish an overall plan for the administration of ongoing research projects.
- Serve as the contact person for study participants, research personnel, work study students, and investigators.
- Maintain relationships and encourage collaborative research with multiple clinicians and researchers.
- Assist in the preparation of manuscripts and presentations.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
No Education Listed
