Specialty Coordinator, Nurse Practitioner

Primary responsibility for the clinical care of patients enrolled in a Phase 1 industry sponsored drug trial

ESSENTIAL JOB DUTIES:

* Oversee patient management during trial in compliance with study protocol

* Assist with administration of Investigational Product

* Assist with patient monitoring before, during, and after administration of investigational product

* Ensure that all study-related procedures are performed in compliance with study protocol

* Work closely with study coordinator to manage and coordinate visits for study participants

* Work with study monitors

* Clinical data entry during trial

* Completes all required compliance coursework

* Reports to study Principal Investigator

* Performs other duties, as assigned

The candidate must possess excellent interpersonal and communication skills, as the position involves extensive interaction with patients, researchers, physicians, and clinical staff. He/she should be capable of performing both independently and as part of a team, demonstrating the ability to multi-task and take initiative. Strong organizational skills and attention to detail are essential for data collection and entry. The position also requires training in Institutional Review Board (IRB) protocols, HIPAA and human subject research. FNP/ANP