Melanoma Clinical Research Coordinator (Part-Time)

The University of North Carolina at Chapel Hill; North Carolina; On-site; USD 28,000 - 40,000; Part time

Job summary

The University of North Carolina at Chapel Hill invites applications for an Associate Clinical Research Coordinator to work on melanoma clinical research projects. The role involves coordinating protocols, collecting and reporting data, and maintaining the UNC Melanoma and Complex Skin Cancer Registry, while adhering to HIPAA and CITI requirements.

The successful candidate will recruit eligible populations, liaise with investigators and staff, support manuscript preparation, and help ensure

Qualifications

• Bachelor's degree; or equivalent combination of training and experience. All degrees must be received from appropriately accredited institutions.
• Experience initiating and updating IRB and PRC applications.
• Experience in an oncology-related field.
• Ability to communicate through various forms with multiple researchers.

Responsibilities

• Execute clinical research protocols for melanoma projects and gather, compile, and report data.
• Maintain the UNC Melanoma and Complex Skin Cancer Registry and other cancer study databases.
• Identify and recruit eligible populations; liaise with investigators, data managers, and study staff.
• Assist in manuscript preparation and presentations; ensure regulatory compliance.

Skills

IRB submissions

PRC applications

oncology experience

Epic@UNC

REDCap

MS Access

Microsoft Office

communication with researchers

Education

Bachelor's degree

Tools

Epic@UNC

REDCap

MS Access

Microsoft Office

Job description

The University of North Carolina at Chapel Hill invites applications for an Associate Clinical Research Coordinator to work on melanoma clinical research projects. The role involves coordinating protocols, collecting and reporting data, and maintaining the UNC Melanoma and Complex Skin Cancer Registry, while adhering to HIPAA and CITI requirements.

The successful candidate will recruit eligible populations, liaise with investigators and staff, support manuscript preparation, and help ensure