Study Coordinator

Position Summary

This position plays a pivotal role in advancing cancer research and improving patient outcomes by facilitating the conduct of oncology clinical trials in compliance with federal regulations, Good Clinical Practice, and institutional policies. This position independently manages multiple complex trials throughout their life cycle, including activation, implementation, and closure, under the direction of a Clinical Operations Manager.

Key responsibilities include: Recruitment, consent, and enrollment of study participants; Coordination of study visits across various clinic settings; Documentation of procedures and visits, facilitation of sample collection, and data entry; Collaboration with research teams to ensure regulatory compliance and patient safety.

Minimum Education and Experience Requirements

Bachelor’s degree in a discipline related to the field assigned and one year of related training or experience; or equivalent combination of training and experience. All degrees must be received from appropriately accredited institutions.