Clinical Research Coordinator - Comprehensive Cancer Center

Position Summary

The Clinical Research Coordinator plays a crucial role in coordinating daily activities and efforts related to the Center for Cancer Prevention and Surviorship. The individual will primarily focus on facilitating clinical research projects in areas such as cancer prevention and control and dietary and physical activity interventions.

Responsibilities

• Assist with research projects, such as participants recruitment, informed consent, scheduling, assessments, data collection, monitor and document adverse events to behavioral intervention

• Assist with behavioral intervention development and delivery

• Assist with developing and managing regulatory protocols. Support activities to ensure compliance with all Institutional Review Boards (IRB), federal, state, and industry sponsor regulations

• Assist with coordinating and preparing for external quality assurance and control reviews by IRB, federal or industry sponsors

• Assist with collaborations within and across departments to develop new research projects

• Conducts scientific literature reviews, systematic reviews, and assists in drafting manuscripts, analyzing relevant research to support the development of scientific publications

• Performs accurate medical chart reviews and data abstraction from EHRs, ensuring meticulous record-keeping in accordance with established protocols

• Attends study meetings and provides regular updates on study progress

• Submission (not writing) of scientific manuscripts

• Excellent communication and writing skills

• Highly organized and self-driven

Job Requirements
Bachelors Degree in Biological Sciences, Health Sciences, Social Sciences or other medical field, or equivalent combination of education experience required. 1 year of relevant experience required.

Research and Scholarship - Clinical Research - Individual Contributor - Specialized - S2