Conducts research assessments on study participants. Assists with and adheres to Institutional Review Board (IRB) renewal, modification, and approved protocols. Assists with training staff. Ensures adherence to protocols and corrects issues with data collection.

Conducts research assessments on study participants. Assists with and adheres to Institutional Review Board (IRB) renewal, modification, and approved protocols. Assists with training staff. Ensures adherence to protocols and corrects issues with data collection.

This coordinator will do all Coordinating functions (screening patients, reviewing consent, obtaining data for study, working in databases, collecting research documents as required by protocols, working with patients and families on floors, data collection). This position would require the individual to understand IT and how to manage different interfaces.

Need to have a good understanding on clinical process and pathways. Will also be responsible for interfacing, data collection and statistical outcomes.