Oncology Clinical Trials Study Coordinator

The University of North Carolina at Chapel Hill; Chapel Hill (NC); Presencial; USD 64 000 - 75 000; Tempo integral

Resumo da oferta

The University of North Carolina at Chapel Hill is seeking a Study Coordinator to advance cancer research by facilitating oncology clinical trials in compliance with federal regulations and institutional policies. The role manages multiple trials across activation, implementation, and closure under supervision, supporting patient care and data integrity.

Based in Chapel Hill, this full-time position requires coordination with clinical teams, recruitment and enrollment of participants, and

Qualificações

• Bachelor’s degree and at least one year of related training or experience.
• Experience as a study coordinator or in oncology clinical trials.
• Knowledge of ICH GCP and federal regulations.
• SOCRA or ACRP certification preferred.

Responsabilidades

• Recruitment, consent, and enrollment of study participants.
• Coordinate study visits across clinic settings.
• Document procedures and visits; facilitate sample collection and data entry.
• Ensure regulatory compliance and patient safety with research teams.

Conhecimentos

Study coordination

Regulatory compliance

Data management

Communication

Team collaboration

Formação académica

Bachelor's degree in a related field

Descrição da oferta de emprego

The University of North Carolina at Chapel Hill is seeking a Study Coordinator to advance cancer research by facilitating oncology clinical trials in compliance with federal regulations and institutional policies. The role manages multiple trials across activation, implementation, and closure under supervision, supporting patient care and data integrity.

Based in Chapel Hill, this full-time position requires coordination with clinical teams, recruitment and enrollment of participants, and