Clinical Research Coordinator (Oncology)
Hybrid
Core
Administratively coordinate clinical protocol implementation and provide logistical support for research-related regulatory issues in oncology studies.
Role type
Clinical Research Coordinator
Builds
Clinical research studies for disease prevention and treatment
Domain
Healthcare / Oncology
Required skills
Protocol adherence, participant recruitment, informed consent administration, data entry, IRB liaison, budget management, sample handling
Preferred skills
Clinical equipment operation, literature search
Responsibilities
Coordinate clinical research study activities, conduct participant recruitment, manage informed consent process, enter and organize study data, liaise with IRB, oversee study budget, handle biological samples