Clinical Research Assistant-235861

SEEKING A CLINICAL RESEARCH ASSISTANT IN MADISON, MISSISSIPPI

The research assistant is primarily responsible for assisting in research patient visits according to International Council for Harmonisation Good Clinical Practice (ICH-GCP) guidelines and according to the Institutional Review Board (IRB)-approved study protocol and / or manual of procedures. Day-to-day activities may include all or some of the essential functions listed below, depending upon individual experience / knowledge and the needs of the organization which are subject to change from time to time.

Duties :

• Coordinate and schedule subject visits within study / subject specific windows per protocol

guidelines.

medications, etc.) study visits (Phase 2 & 3; NO Gene Therapy)

protocol