The Clinical Research Associate will monitor activities at our clinical study sites to assure adherence to federal regulations, Good Clinical Practices (GCPs), Standards of Procedures (SOPs), and study protocols. Travel approximately 25 - 35% of time. When not traveling, CRA will work in-house generating clinical documents, entering and managing trial data, and supporting all functions of clinical trial management.   This is in-house position.

Qualifications:
BS/BA or equivalent combination of education and experience in a healthcare or scientific discipline preferred ; strong understanding of Medical Terminology; strong organizational skills; excellent written and verbal communication skills; must be computer literate and proficient in MS office. Ability to work independently and take direction from others.